Name: rs71149066
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs71149066

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:30884493-30884514 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₃ / del(T)₁₁ / del(T)₈ / de…
del(T)₁₃ / del(T)₁₁ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₃=0.000015 (4/264690, TOPMED)
dupTT=0.00666 (116/17421, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BCL7C : Intron Variant
MIR762HG : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20230706150541

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	17421	TTTTTTTTTTTTTTTTTTTTTT=0.98818	TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00034, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00253, TTTTTTTTTTTTTTTTTTTTTTT=0.00166, TTTTTTTTTTTTTTTTTTTTTTTT=0.00666, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00063
European	Sub	13547	TTTTTTTTTTTTTTTTTTTTTT=0.98494	TTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00044, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00317, TTTTTTTTTTTTTTTTTTTTTTT=0.00214, TTTTTTTTTTTTTTTTTTTTTTTT=0.00849, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00081
African	Sub	2488	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000
African Others	Sub	94	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00
African American	Sub	2394	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000
Asian	Sub	112	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000
East Asian	Sub	86	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00
Latin American 1	Sub	130	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000
Latin American 2	Sub	574	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000
South Asian	Sub	96	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00
Other	Sub	474	TTTTTTTTTTTTTTTTTTTTTT=0.996	TTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.002, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.002, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₂₂=0.999985	del(T)₁₃=0.000015
Allele Frequency Aggregator	Total	Global	17421	(T)₂₂=0.98818	del(T)₁₃=0.00000, del(T)₁₁=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00034, delTT=0.00000, delT=0.00253, dupT=0.00166, dupTT=0.00666, dupTTT=0.00063
Allele Frequency Aggregator	European	Sub	13547	(T)₂₂=0.98494	del(T)₁₃=0.00000, del(T)₁₁=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00044, delTT=0.00000, delT=0.00317, dupT=0.00214, dupTT=0.00849, dupTTT=0.00081
Allele Frequency Aggregator	African	Sub	2488	(T)₂₂=1.0000	del(T)₁₃=0.0000, del(T)₁₁=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	574	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	474	(T)₂₂=0.996	del(T)₁₃=0.000, del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.002, dupT=0.000, dupTT=0.002, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	130	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₂₂=1.000	del(T)₁₃=0.000, del(T)₁₁=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	96	(T)₂₂=1.00	del(T)₁₃=0.00, del(T)₁₁=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 16	NC_000016.10:g.30884502_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884504_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884507_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884508_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884509_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884510_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884512_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884513_30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884514del
GRCh38.p14 chr 16	NC_000016.10:g.30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884513_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884512_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884511_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884510_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884509_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884508_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884507_30884514dup
GRCh38.p14 chr 16	NC_000016.10:g.30884504_30884514dup
GRCh37.p13 chr 16	NC_000016.9:g.30895823_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895825_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895828_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895829_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895830_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895831_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895833_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895834_30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895835del
GRCh37.p13 chr 16	NC_000016.9:g.30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895834_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895833_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895832_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895831_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895830_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895829_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895828_30895835dup
GRCh37.p13 chr 16	NC_000016.9:g.30895825_30895835dup

Gene: BCL7C, BAF chromatin remodeling complex subunit BCL7C (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BCL7C transcript variant 1	NM_001286526.2:c.528+4355… NM_001286526.2:c.528+4355_528+4367del	N/A	Intron Variant
BCL7C transcript variant 2	NM_004765.4:c.	N/A	Genic Downstream Transcript Variant
BCL7C transcript variant X2	XM_011545980.4:c.528+4355… XM_011545980.4:c.528+4355_528+4367del	N/A	Intron Variant
BCL7C transcript variant X1	XM_047434896.1:c.529-4189… XM_047434896.1:c.529-4189_529-4177del	N/A	Intron Variant
BCL7C transcript variant X3	XM_047434897.1:c.429+4355… XM_047434897.1:c.429+4355_429+4367del	N/A	Intron Variant
BCL7C transcript variant X4	XM_047434898.1:c.330+4355… XM_047434898.1:c.330+4355_330+4367del	N/A	Intron Variant
BCL7C transcript variant X5	XM_047434899.1:c.	N/A	Genic Downstream Transcript Variant
BCL7C transcript variant X6	XM_047434900.1:c.	N/A	Genic Downstream Transcript Variant

Gene: MIR762HG, MIR762 host gene (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MIR762HG transcript variant 1	NR_110940.1:n.	N/A	Intron Variant
MIR762HG transcript variant 2	NR_110941.1:n.	N/A	Intron Variant
MIR762HG transcript variant 3	NR_110942.1:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₂=	del(T)₁₃	del(T)₁₁	del(T)₈	del(T)₇	del(T)₆	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₁
GRCh38.p14 chr 16	NC_000016.10:g.30884493_30884514=	NC_000016.10:g.30884502_30884514del	NC_000016.10:g.30884504_30884514del	NC_000016.10:g.30884507_30884514del	NC_000016.10:g.30884508_30884514del	NC_000016.10:g.30884509_30884514del	NC_000016.10:g.30884510_30884514del	NC_000016.10:g.30884512_30884514del	NC_000016.10:g.30884513_30884514del	NC_000016.10:g.30884514del	NC_000016.10:g.30884514dup	NC_000016.10:g.30884513_30884514dup	NC_000016.10:g.30884512_30884514dup	NC_000016.10:g.30884511_30884514dup	NC_000016.10:g.30884510_30884514dup	NC_000016.10:g.30884509_30884514dup	NC_000016.10:g.30884508_30884514dup	NC_000016.10:g.30884507_30884514dup	NC_000016.10:g.30884504_30884514dup
GRCh37.p13 chr 16	NC_000016.9:g.30895814_30895835=	NC_000016.9:g.30895823_30895835del	NC_000016.9:g.30895825_30895835del	NC_000016.9:g.30895828_30895835del	NC_000016.9:g.30895829_30895835del	NC_000016.9:g.30895830_30895835del	NC_000016.9:g.30895831_30895835del	NC_000016.9:g.30895833_30895835del	NC_000016.9:g.30895834_30895835del	NC_000016.9:g.30895835del	NC_000016.9:g.30895835dup	NC_000016.9:g.30895834_30895835dup	NC_000016.9:g.30895833_30895835dup	NC_000016.9:g.30895832_30895835dup	NC_000016.9:g.30895831_30895835dup	NC_000016.9:g.30895830_30895835dup	NC_000016.9:g.30895829_30895835dup	NC_000016.9:g.30895828_30895835dup	NC_000016.9:g.30895825_30895835dup
BCL7C transcript variant 1	NM_001286526.2:c.528+4367=	NM_001286526.2:c.528+4355_528+4367del	NM_001286526.2:c.528+4357_528+4367del	NM_001286526.2:c.528+4360_528+4367del	NM_001286526.2:c.528+4361_528+4367del	NM_001286526.2:c.528+4362_528+4367del	NM_001286526.2:c.528+4363_528+4367del	NM_001286526.2:c.528+4365_528+4367del	NM_001286526.2:c.528+4366_528+4367del	NM_001286526.2:c.528+4367del	NM_001286526.2:c.528+4367dup	NM_001286526.2:c.528+4366_528+4367dup	NM_001286526.2:c.528+4365_528+4367dup	NM_001286526.2:c.528+4364_528+4367dup	NM_001286526.2:c.528+4363_528+4367dup	NM_001286526.2:c.528+4362_528+4367dup	NM_001286526.2:c.528+4361_528+4367dup	NM_001286526.2:c.528+4360_528+4367dup	NM_001286526.2:c.528+4357_528+4367dup
BCL7C transcript variant X1	XM_005255693.1:c.528+4367=	XM_005255693.1:c.528+4355_528+4367del	XM_005255693.1:c.528+4357_528+4367del	XM_005255693.1:c.528+4360_528+4367del	XM_005255693.1:c.528+4361_528+4367del	XM_005255693.1:c.528+4362_528+4367del	XM_005255693.1:c.528+4363_528+4367del	XM_005255693.1:c.528+4365_528+4367del	XM_005255693.1:c.528+4366_528+4367del	XM_005255693.1:c.528+4367del	XM_005255693.1:c.528+4367dup	XM_005255693.1:c.528+4366_528+4367dup	XM_005255693.1:c.528+4365_528+4367dup	XM_005255693.1:c.528+4364_528+4367dup	XM_005255693.1:c.528+4363_528+4367dup	XM_005255693.1:c.528+4362_528+4367dup	XM_005255693.1:c.528+4361_528+4367dup	XM_005255693.1:c.528+4360_528+4367dup	XM_005255693.1:c.528+4357_528+4367dup
BCL7C transcript variant X2	XM_011545980.4:c.528+4367=	XM_011545980.4:c.528+4355_528+4367del	XM_011545980.4:c.528+4357_528+4367del	XM_011545980.4:c.528+4360_528+4367del	XM_011545980.4:c.528+4361_528+4367del	XM_011545980.4:c.528+4362_528+4367del	XM_011545980.4:c.528+4363_528+4367del	XM_011545980.4:c.528+4365_528+4367del	XM_011545980.4:c.528+4366_528+4367del	XM_011545980.4:c.528+4367del	XM_011545980.4:c.528+4367dup	XM_011545980.4:c.528+4366_528+4367dup	XM_011545980.4:c.528+4365_528+4367dup	XM_011545980.4:c.528+4364_528+4367dup	XM_011545980.4:c.528+4363_528+4367dup	XM_011545980.4:c.528+4362_528+4367dup	XM_011545980.4:c.528+4361_528+4367dup	XM_011545980.4:c.528+4360_528+4367dup	XM_011545980.4:c.528+4357_528+4367dup
BCL7C transcript variant X1	XM_047434896.1:c.529-4177=	XM_047434896.1:c.529-4189_529-4177del	XM_047434896.1:c.529-4187_529-4177del	XM_047434896.1:c.529-4184_529-4177del	XM_047434896.1:c.529-4183_529-4177del	XM_047434896.1:c.529-4182_529-4177del	XM_047434896.1:c.529-4181_529-4177del	XM_047434896.1:c.529-4179_529-4177del	XM_047434896.1:c.529-4178_529-4177del	XM_047434896.1:c.529-4177del	XM_047434896.1:c.529-4177dup	XM_047434896.1:c.529-4178_529-4177dup	XM_047434896.1:c.529-4179_529-4177dup	XM_047434896.1:c.529-4180_529-4177dup	XM_047434896.1:c.529-4181_529-4177dup	XM_047434896.1:c.529-4182_529-4177dup	XM_047434896.1:c.529-4183_529-4177dup	XM_047434896.1:c.529-4184_529-4177dup	XM_047434896.1:c.529-4187_529-4177dup
BCL7C transcript variant X3	XM_047434897.1:c.429+4367=	XM_047434897.1:c.429+4355_429+4367del	XM_047434897.1:c.429+4357_429+4367del	XM_047434897.1:c.429+4360_429+4367del	XM_047434897.1:c.429+4361_429+4367del	XM_047434897.1:c.429+4362_429+4367del	XM_047434897.1:c.429+4363_429+4367del	XM_047434897.1:c.429+4365_429+4367del	XM_047434897.1:c.429+4366_429+4367del	XM_047434897.1:c.429+4367del	XM_047434897.1:c.429+4367dup	XM_047434897.1:c.429+4366_429+4367dup	XM_047434897.1:c.429+4365_429+4367dup	XM_047434897.1:c.429+4364_429+4367dup	XM_047434897.1:c.429+4363_429+4367dup	XM_047434897.1:c.429+4362_429+4367dup	XM_047434897.1:c.429+4361_429+4367dup	XM_047434897.1:c.429+4360_429+4367dup	XM_047434897.1:c.429+4357_429+4367dup
BCL7C transcript variant X4	XM_047434898.1:c.330+4367=	XM_047434898.1:c.330+4355_330+4367del	XM_047434898.1:c.330+4357_330+4367del	XM_047434898.1:c.330+4360_330+4367del	XM_047434898.1:c.330+4361_330+4367del	XM_047434898.1:c.330+4362_330+4367del	XM_047434898.1:c.330+4363_330+4367del	XM_047434898.1:c.330+4365_330+4367del	XM_047434898.1:c.330+4366_330+4367del	XM_047434898.1:c.330+4367del	XM_047434898.1:c.330+4367dup	XM_047434898.1:c.330+4366_330+4367dup	XM_047434898.1:c.330+4365_330+4367dup	XM_047434898.1:c.330+4364_330+4367dup	XM_047434898.1:c.330+4363_330+4367dup	XM_047434898.1:c.330+4362_330+4367dup	XM_047434898.1:c.330+4361_330+4367dup	XM_047434898.1:c.330+4360_330+4367dup	XM_047434898.1:c.330+4357_330+4367dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

41 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95676233	Feb 13, 2009 (130)
2	SSIP	ss947355216	Aug 21, 2014 (142)
3	SWEGEN	ss3014332992	Nov 08, 2017 (151)
4	MCHAISSO	ss3064683316	Nov 08, 2017 (151)
5	EVA	ss3834546415	Apr 27, 2020 (154)
6	KOGIC	ss3977408820	Apr 27, 2020 (154)
7	KOGIC	ss3977408821	Apr 27, 2020 (154)
8	KOGIC	ss3977408822	Apr 27, 2020 (154)
9	KOGIC	ss3977408823	Apr 27, 2020 (154)
10	GNOMAD	ss4299507776	Apr 27, 2021 (155)
11	GNOMAD	ss4299507777	Apr 27, 2021 (155)
12	GNOMAD	ss4299507778	Apr 27, 2021 (155)
13	GNOMAD	ss4299507779	Apr 27, 2021 (155)
14	GNOMAD	ss4299507780	Apr 27, 2021 (155)
15	GNOMAD	ss4299507781	Apr 27, 2021 (155)
16	GNOMAD	ss4299507782	Apr 27, 2021 (155)
17	GNOMAD	ss4299507783	Apr 27, 2021 (155)
18	GNOMAD	ss4299507784	Apr 27, 2021 (155)
19	GNOMAD	ss4299507785	Apr 27, 2021 (155)
20	GNOMAD	ss4299507786	Apr 27, 2021 (155)
21	GNOMAD	ss4299507787	Apr 27, 2021 (155)
22	GNOMAD	ss4299507788	Apr 27, 2021 (155)
23	GNOMAD	ss4299507789	Apr 27, 2021 (155)
24	GNOMAD	ss4299507790	Apr 27, 2021 (155)
25	GNOMAD	ss4299507791	Apr 27, 2021 (155)
26	TOPMED	ss5012812175	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5219190206	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5219190207	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5219190208	Apr 27, 2021 (155)
30	1000G_HIGH_COVERAGE	ss5300685147	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5300685148	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5300685149	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5494110820	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5494110821	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5494110822	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5494110823	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5773897779	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5773897780	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5773897781	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5773897782	Oct 16, 2022 (156)
41	EVA	ss5851549111	Oct 16, 2022 (156)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487277281 (NC_000016.10:30884492::T 1505/90422) Row 487277282 (NC_000016.10:30884492::TT 2227/90372) Row 487277283 (NC_000016.10:30884492::TTT 173/90454)...	-	Apr 27, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 33786821 (NC_000016.10:30884494::T 200/1824) Row 33786822 (NC_000016.10:30884494::TT 75/1824) Row 33786823 (NC_000016.10:30884493:T: 190/1824)...	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 33786821 (NC_000016.10:30884494::T 200/1824) Row 33786822 (NC_000016.10:30884494::TT 75/1824) Row 33786823 (NC_000016.10:30884493:T: 190/1824)...	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 33786821 (NC_000016.10:30884494::T 200/1824) Row 33786822 (NC_000016.10:30884494::TT 75/1824) Row 33786823 (NC_000016.10:30884493:T: 190/1824)...	-	Apr 27, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 33786821 (NC_000016.10:30884494::T 200/1824) Row 33786822 (NC_000016.10:30884494::TT 75/1824) Row 33786823 (NC_000016.10:30884493:T: 190/1824)...	-	Apr 27, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 77159513 (NC_000016.9:30895813::T 113/16722) Row 77159514 (NC_000016.9:30895813:T: 18/16722) Row 77159515 (NC_000016.9:30895813::TT 72/16722)	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 77159513 (NC_000016.9:30895813::T 113/16722) Row 77159514 (NC_000016.9:30895813:T: 18/16722) Row 77159515 (NC_000016.9:30895813::TT 72/16722)	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 77159513 (NC_000016.9:30895813::T 113/16722) Row 77159514 (NC_000016.9:30895813:T: 18/16722) Row 77159515 (NC_000016.9:30895813::TT 72/16722)	-	Apr 27, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 107734883 (NC_000016.10:30884492::T 157/27896) Row 107734884 (NC_000016.10:30884492:T: 29/27896) Row 107734885 (NC_000016.10:30884492::TT 113/27896)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 107734883 (NC_000016.10:30884492::T 157/27896) Row 107734884 (NC_000016.10:30884492:T: 29/27896) Row 107734885 (NC_000016.10:30884492::TT 113/27896)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 107734883 (NC_000016.10:30884492::T 157/27896) Row 107734884 (NC_000016.10:30884492:T: 29/27896) Row 107734885 (NC_000016.10:30884492::TT 113/27896)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 107734883 (NC_000016.10:30884492::T 157/27896) Row 107734884 (NC_000016.10:30884492:T: 29/27896) Row 107734885 (NC_000016.10:30884492::TT 113/27896)...	-	Oct 16, 2022 (156)
69	TopMed	NC_000016.10 - 30884493	Apr 27, 2021 (155)
70	ALFA	NC_000016.10 - 30884493	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
228357836, ss5012812175	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4299507791	NC_000016.10:30884492:TTTTTTTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3014332992	NC_000016.9:30895813:TTTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4299507790, ss5494110823, ss5851549111	NC_000016.10:30884492:TTTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4299507789	NC_000016.10:30884492:TTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4299507788	NC_000016.10:30884492:TTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4299507787	NC_000016.10:30884492:TTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3977408823, ss4299507786	NC_000016.10:30884492:TT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5219190207	NC_000016.9:30895813:T:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507785, ss5300685148, ss5494110821, ss5773897780	NC_000016.10:30884492:T:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3977408822	NC_000016.10:30884493:T:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95676233	NT_010393.16:30835834:T:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5219190206	NC_000016.9:30895813::T	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss947355216	NC_000016.9:30895814::T	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507776, ss5300685149, ss5494110822, ss5773897779	NC_000016.10:30884492::T	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3977408820	NC_000016.10:30884494::T	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3834546415, ss5219190208	NC_000016.9:30895813::TT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3064683316, ss4299507777, ss5300685147, ss5494110820, ss5773897781	NC_000016.10:30884492::TT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3977408821	NC_000016.10:30884494::TT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507778, ss5773897782	NC_000016.10:30884492::TTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6179722343	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507779	NC_000016.10:30884492::TTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507780	NC_000016.10:30884492::TTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507781	NC_000016.10:30884492::TTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507782	NC_000016.10:30884492::TTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507783	NC_000016.10:30884492::TTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4299507784	NC_000016.10:30884492::TTTTTTTTTTT	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2376522370	NC_000016.9:30895813:TTTTTTTTTTTTT:	NC_000016.10:30884492:TTTTTTTTTTTT… NC_000016.10:30884492:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs71149066

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71149066