Name: rs35651129
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.

rs35651129

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:72007028-72007035 (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: delA / dupA / dupAA / ins(A)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.135135 (35769/264690, TOPMED)
dupA=0.05630 (745/13232, ALFA)
dupA=0.1510 (756/5008, 1000G) (+ 7 more)
dupA=0.1659 (743/4478, Estonian)
dupA=0.1614 (622/3854, ALSPAC)
dupA=0.1742 (646/3708, TWINSUK)
dupA=0.1878 (344/1832, Korea1K)
dupA=0.172 (172/998, GoNL)
dupA=0.196 (117/598, NorthernSweden)
dupA=0.15 (6/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RGS6 : 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	13232	AAAAAAAA=0.94362	AAAAAAA=0.00000, AAAAAAAAA=0.05630, AAAAAAAAAAAAAAAAA=0.00008, AAAAAAAAAA=0.00000
European	Sub	9726	AAAAAAAA=0.9235	AAAAAAA=0.0000, AAAAAAAAA=0.0764, AAAAAAAAAAAAAAAAA=0.0001, AAAAAAAAAA=0.0000
African	Sub	2548	AAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAA=0.0000
African Others	Sub	102	AAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAA=0.000
African American	Sub	2446	AAAAAAAA=1.0000	AAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAA=0.0000
Asian	Sub	72	AAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAA=0.00
East Asian	Sub	52	AAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAA=0.00
Other Asian	Sub	20	AAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAA=0.00
Latin American 1	Sub	104	AAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAA=0.000
Latin American 2	Sub	354	AAAAAAAA=1.000	AAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAA=0.000
South Asian	Sub	62	AAAAAAAA=1.00	AAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAA=0.00
Other	Sub	366	AAAAAAAA=0.995	AAAAAAA=0.000, AAAAAAAAA=0.005, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAA=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	- No frequency provided	dupA=0.135135
Allele Frequency Aggregator	Total	Global	13232	(A)₈=0.94362	delA=0.00000, dupA=0.05630, dupAA=0.00000, ins(A)₉=0.00008
Allele Frequency Aggregator	European	Sub	9726	(A)₈=0.9235	delA=0.0000, dupA=0.0764, dupAA=0.0000, ins(A)₉=0.0001
Allele Frequency Aggregator	African	Sub	2548	(A)₈=1.0000	delA=0.0000, dupA=0.0000, dupAA=0.0000, ins(A)₉=0.0000
Allele Frequency Aggregator	Other	Sub	366	(A)₈=0.995	delA=0.000, dupA=0.005, dupAA=0.000, ins(A)₉=0.000
Allele Frequency Aggregator	Latin American 2	Sub	354	(A)₈=1.000	delA=0.000, dupA=0.000, dupAA=0.000, ins(A)₉=0.000
Allele Frequency Aggregator	Latin American 1	Sub	104	(A)₈=1.000	delA=0.000, dupA=0.000, dupAA=0.000, ins(A)₉=0.000
Allele Frequency Aggregator	Asian	Sub	72	(A)₈=1.00	delA=0.00, dupA=0.00, dupAA=0.00, ins(A)₉=0.00
Allele Frequency Aggregator	South Asian	Sub	62	(A)₈=1.00	delA=0.00, dupA=0.00, dupAA=0.00, ins(A)₉=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.1510
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.0446
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.1935
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.1710
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.182
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.219
Genetic variation in the Estonian population	Estonian	Study-wide	4478	- No frequency provided	dupA=0.1659
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupA=0.1614
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupA=0.1742
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupA=0.1878
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	- No frequency provided	dupA=0.172
Northern Sweden	ACPOP	Study-wide	598	- No frequency provided	dupA=0.196
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.15

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 14	NC_000014.9:g.72007035del
GRCh38.p14 chr 14	NC_000014.9:g.72007035dup
GRCh38.p14 chr 14	NC_000014.9:g.72007034_72007035dup
GRCh38.p14 chr 14	NC_000014.9:g.72007035_72007036insAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.72473752del
GRCh37.p13 chr 14	NC_000014.8:g.72473752dup
GRCh37.p13 chr 14	NC_000014.8:g.72473751_72473752dup
GRCh37.p13 chr 14	NC_000014.8:g.72473752_72473753insAAAAAAAAA
RGS6 RefSeqGene	NG_029236.1:g.79936del
RGS6 RefSeqGene	NG_029236.1:g.79936dup
RGS6 RefSeqGene	NG_029236.1:g.79935_79936dup
RGS6 RefSeqGene	NG_029236.1:g.79936_79937insAAAAAAAAA

Gene: RGS6, regulator of G protein signaling 6 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RGS6 transcript variant 1	NM_001204416.3:c.84+42160… NM_001204416.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 3	NM_001204417.3:c.84+42160… NM_001204417.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 4	NM_001204418.3:c.84+42160… NM_001204418.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 5	NM_001204419.3:c.84+42160… NM_001204419.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 6	NM_001204420.3:c.84+42160… NM_001204420.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 7	NM_001204421.3:c.84+42160… NM_001204421.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 8	NM_001204422.3:c.84+42160… NM_001204422.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 9	NM_001204423.2:c.-22+7480… NM_001204423.2:c.-22+74802del	N/A	Intron Variant
RGS6 transcript variant 10	NM_001204424.2:c.84+42160… NM_001204424.2:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 12	NM_001370270.1:c.84+42160… NM_001370270.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 13	NM_001370271.1:c.84+42160… NM_001370271.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 14	NM_001370272.1:c.84+42160… NM_001370272.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 15	NM_001370273.1:c.84+42160… NM_001370273.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 16	NM_001370274.1:c.84+42160… NM_001370274.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 17	NM_001370275.1:c.84+42160… NM_001370275.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 18	NM_001370276.1:c.84+42160… NM_001370276.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 19	NM_001370277.1:c.84+42160… NM_001370277.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 20	NM_001370278.1:c.84+42160… NM_001370278.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 21	NM_001370279.1:c.84+42160… NM_001370279.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 22	NM_001370280.1:c.84+42160… NM_001370280.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 23	NM_001370281.1:c.84+42160… NM_001370281.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 24	NM_001370282.1:c.84+42160… NM_001370282.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 25	NM_001370283.1:c.84+42160… NM_001370283.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 26	NM_001370284.1:c.84+42160… NM_001370284.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 27	NM_001370286.1:c.84+42160… NM_001370286.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 28	NM_001370287.1:c.84+42160… NM_001370287.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 29	NM_001370288.1:c.84+42160… NM_001370288.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 30	NM_001370289.1:c.84+42160… NM_001370289.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 31	NM_001370290.1:c.84+42160… NM_001370290.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 32	NM_001370291.1:c.84+42160… NM_001370291.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 33	NM_001370292.1:c.84+42160… NM_001370292.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 34	NM_001370293.1:c.84+42160… NM_001370293.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 35	NM_001370294.1:c.84+42160… NM_001370294.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 2	NM_004296.7:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant 11	NR_135235.2:n.	N/A	Intron Variant
RGS6 transcript variant X4	XM_017021820.3:c.84+42160… XM_017021820.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X9	XM_017021822.3:c.84+42160… XM_017021822.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X11	XM_017021825.3:c.84+42160… XM_017021825.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X12	XM_017021826.3:c.84+42160… XM_017021826.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X13	XM_017021827.3:c.84+42160… XM_017021827.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X15	XM_017021828.3:c.84+42160… XM_017021828.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X16	XM_017021830.3:c.84+42160… XM_017021830.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X17	XM_017021831.3:c.84+42160… XM_017021831.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X18	XM_017021832.3:c.84+42160… XM_017021832.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X21	XM_017021833.3:c.84+42160… XM_017021833.3:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X1	XM_024449759.2:c.84+42160… XM_024449759.2:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X3	XM_024449760.2:c.84+42160… XM_024449760.2:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X2	XM_024449761.2:c.84+42160… XM_024449761.2:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X19	XM_024449776.2:c.84+42160… XM_024449776.2:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X10	XM_047431987.1:c.84+42160… XM_047431987.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X20	XM_047431990.1:c.84+42160… XM_047431990.1:c.84+42160del	N/A	Intron Variant
RGS6 transcript variant X8	XM_011537397.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X6	XM_024449763.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X7	XM_024449764.2:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X5	XM_047431985.1:c.	N/A	Genic Upstream Transcript Variant
RGS6 transcript variant X14	XM_047431988.1:c.	N/A	Genic Upstream Transcript 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	(A)₈=	delA	dupA	dupAA	ins(A)₉
GRCh38.p14 chr 14	NC_000014.9:g.72007028_72007035=	NC_000014.9:g.72007035del	NC_000014.9:g.72007035dup	NC_000014.9:g.72007034_72007035dup	NC_000014.9:g.72007035_72007036insAAAAAAAAA
GRCh37.p13 chr 14	NC_000014.8:g.72473745_72473752=	NC_000014.8:g.72473752del	NC_000014.8:g.72473752dup	NC_000014.8:g.72473751_72473752dup	NC_000014.8:g.72473752_72473753insAAAAAAAAA
RGS6 RefSeqGene	NG_029236.1:g.79929_79936=	NG_029236.1:g.79936del	NG_029236.1:g.79936dup	NG_029236.1:g.79935_79936dup	NG_029236.1:g.79936_79937insAAAAAAAAA
RGS6 transcript variant 1	NM_001204416.1:c.84+42153=	NM_001204416.1:c.84+42160del	NM_001204416.1:c.84+42160dup	NM_001204416.1:c.84+42159_84+42160dup	NM_001204416.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 1	NM_001204416.3:c.84+42153=	NM_001204416.3:c.84+42160del	NM_001204416.3:c.84+42160dup	NM_001204416.3:c.84+42159_84+42160dup	NM_001204416.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 3	NM_001204417.1:c.84+42153=	NM_001204417.1:c.84+42160del	NM_001204417.1:c.84+42160dup	NM_001204417.1:c.84+42159_84+42160dup	NM_001204417.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 3	NM_001204417.3:c.84+42153=	NM_001204417.3:c.84+42160del	NM_001204417.3:c.84+42160dup	NM_001204417.3:c.84+42159_84+42160dup	NM_001204417.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 4	NM_001204418.1:c.84+42153=	NM_001204418.1:c.84+42160del	NM_001204418.1:c.84+42160dup	NM_001204418.1:c.84+42159_84+42160dup	NM_001204418.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 4	NM_001204418.3:c.84+42153=	NM_001204418.3:c.84+42160del	NM_001204418.3:c.84+42160dup	NM_001204418.3:c.84+42159_84+42160dup	NM_001204418.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 5	NM_001204419.1:c.84+42153=	NM_001204419.1:c.84+42160del	NM_001204419.1:c.84+42160dup	NM_001204419.1:c.84+42159_84+42160dup	NM_001204419.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 5	NM_001204419.3:c.84+42153=	NM_001204419.3:c.84+42160del	NM_001204419.3:c.84+42160dup	NM_001204419.3:c.84+42159_84+42160dup	NM_001204419.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 6	NM_001204420.1:c.84+42153=	NM_001204420.1:c.84+42160del	NM_001204420.1:c.84+42160dup	NM_001204420.1:c.84+42159_84+42160dup	NM_001204420.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 6	NM_001204420.3:c.84+42153=	NM_001204420.3:c.84+42160del	NM_001204420.3:c.84+42160dup	NM_001204420.3:c.84+42159_84+42160dup	NM_001204420.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 7	NM_001204421.1:c.84+42153=	NM_001204421.1:c.84+42160del	NM_001204421.1:c.84+42160dup	NM_001204421.1:c.84+42159_84+42160dup	NM_001204421.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 7	NM_001204421.3:c.84+42153=	NM_001204421.3:c.84+42160del	NM_001204421.3:c.84+42160dup	NM_001204421.3:c.84+42159_84+42160dup	NM_001204421.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 8	NM_001204422.1:c.84+42153=	NM_001204422.1:c.84+42160del	NM_001204422.1:c.84+42160dup	NM_001204422.1:c.84+42159_84+42160dup	NM_001204422.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 8	NM_001204422.3:c.84+42153=	NM_001204422.3:c.84+42160del	NM_001204422.3:c.84+42160dup	NM_001204422.3:c.84+42159_84+42160dup	NM_001204422.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 9	NM_001204423.1:c.-22+74795=	NM_001204423.1:c.-22+74802del	NM_001204423.1:c.-22+74802dup	NM_001204423.1:c.-22+74801_-22+74802dup	NM_001204423.1:c.-22+74802_-22+74803insAAAAAAAAA
RGS6 transcript variant 9	NM_001204423.2:c.-22+74795=	NM_001204423.2:c.-22+74802del	NM_001204423.2:c.-22+74802dup	NM_001204423.2:c.-22+74801_-22+74802dup	NM_001204423.2:c.-22+74802_-22+74803insAAAAAAAAA
RGS6 transcript variant 10	NM_001204424.1:c.84+42153=	NM_001204424.1:c.84+42160del	NM_001204424.1:c.84+42160dup	NM_001204424.1:c.84+42159_84+42160dup	NM_001204424.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 10	NM_001204424.2:c.84+42153=	NM_001204424.2:c.84+42160del	NM_001204424.2:c.84+42160dup	NM_001204424.2:c.84+42159_84+42160dup	NM_001204424.2:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 12	NM_001370270.1:c.84+42153=	NM_001370270.1:c.84+42160del	NM_001370270.1:c.84+42160dup	NM_001370270.1:c.84+42159_84+42160dup	NM_001370270.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 13	NM_001370271.1:c.84+42153=	NM_001370271.1:c.84+42160del	NM_001370271.1:c.84+42160dup	NM_001370271.1:c.84+42159_84+42160dup	NM_001370271.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 14	NM_001370272.1:c.84+42153=	NM_001370272.1:c.84+42160del	NM_001370272.1:c.84+42160dup	NM_001370272.1:c.84+42159_84+42160dup	NM_001370272.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 15	NM_001370273.1:c.84+42153=	NM_001370273.1:c.84+42160del	NM_001370273.1:c.84+42160dup	NM_001370273.1:c.84+42159_84+42160dup	NM_001370273.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 16	NM_001370274.1:c.84+42153=	NM_001370274.1:c.84+42160del	NM_001370274.1:c.84+42160dup	NM_001370274.1:c.84+42159_84+42160dup	NM_001370274.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 17	NM_001370275.1:c.84+42153=	NM_001370275.1:c.84+42160del	NM_001370275.1:c.84+42160dup	NM_001370275.1:c.84+42159_84+42160dup	NM_001370275.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 18	NM_001370276.1:c.84+42153=	NM_001370276.1:c.84+42160del	NM_001370276.1:c.84+42160dup	NM_001370276.1:c.84+42159_84+42160dup	NM_001370276.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 19	NM_001370277.1:c.84+42153=	NM_001370277.1:c.84+42160del	NM_001370277.1:c.84+42160dup	NM_001370277.1:c.84+42159_84+42160dup	NM_001370277.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 20	NM_001370278.1:c.84+42153=	NM_001370278.1:c.84+42160del	NM_001370278.1:c.84+42160dup	NM_001370278.1:c.84+42159_84+42160dup	NM_001370278.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 21	NM_001370279.1:c.84+42153=	NM_001370279.1:c.84+42160del	NM_001370279.1:c.84+42160dup	NM_001370279.1:c.84+42159_84+42160dup	NM_001370279.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 22	NM_001370280.1:c.84+42153=	NM_001370280.1:c.84+42160del	NM_001370280.1:c.84+42160dup	NM_001370280.1:c.84+42159_84+42160dup	NM_001370280.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 23	NM_001370281.1:c.84+42153=	NM_001370281.1:c.84+42160del	NM_001370281.1:c.84+42160dup	NM_001370281.1:c.84+42159_84+42160dup	NM_001370281.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 24	NM_001370282.1:c.84+42153=	NM_001370282.1:c.84+42160del	NM_001370282.1:c.84+42160dup	NM_001370282.1:c.84+42159_84+42160dup	NM_001370282.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 25	NM_001370283.1:c.84+42153=	NM_001370283.1:c.84+42160del	NM_001370283.1:c.84+42160dup	NM_001370283.1:c.84+42159_84+42160dup	NM_001370283.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 26	NM_001370284.1:c.84+42153=	NM_001370284.1:c.84+42160del	NM_001370284.1:c.84+42160dup	NM_001370284.1:c.84+42159_84+42160dup	NM_001370284.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 27	NM_001370286.1:c.84+42153=	NM_001370286.1:c.84+42160del	NM_001370286.1:c.84+42160dup	NM_001370286.1:c.84+42159_84+42160dup	NM_001370286.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 28	NM_001370287.1:c.84+42153=	NM_001370287.1:c.84+42160del	NM_001370287.1:c.84+42160dup	NM_001370287.1:c.84+42159_84+42160dup	NM_001370287.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 29	NM_001370288.1:c.84+42153=	NM_001370288.1:c.84+42160del	NM_001370288.1:c.84+42160dup	NM_001370288.1:c.84+42159_84+42160dup	NM_001370288.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 30	NM_001370289.1:c.84+42153=	NM_001370289.1:c.84+42160del	NM_001370289.1:c.84+42160dup	NM_001370289.1:c.84+42159_84+42160dup	NM_001370289.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 31	NM_001370290.1:c.84+42153=	NM_001370290.1:c.84+42160del	NM_001370290.1:c.84+42160dup	NM_001370290.1:c.84+42159_84+42160dup	NM_001370290.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 32	NM_001370291.1:c.84+42153=	NM_001370291.1:c.84+42160del	NM_001370291.1:c.84+42160dup	NM_001370291.1:c.84+42159_84+42160dup	NM_001370291.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 33	NM_001370292.1:c.84+42153=	NM_001370292.1:c.84+42160del	NM_001370292.1:c.84+42160dup	NM_001370292.1:c.84+42159_84+42160dup	NM_001370292.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 34	NM_001370293.1:c.84+42153=	NM_001370293.1:c.84+42160del	NM_001370293.1:c.84+42160dup	NM_001370293.1:c.84+42159_84+42160dup	NM_001370293.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 35	NM_001370294.1:c.84+42153=	NM_001370294.1:c.84+42160del	NM_001370294.1:c.84+42160dup	NM_001370294.1:c.84+42159_84+42160dup	NM_001370294.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 2	NM_004296.5:c.84+42153=	NM_004296.5:c.84+42160del	NM_004296.5:c.84+42160dup	NM_004296.5:c.84+42159_84+42160dup	NM_004296.5:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant 2	NM_004296.7:c.84+42153=	NM_004296.7:c.84+42160del	NM_004296.7:c.84+42160dup	NM_004296.7:c.84+42159_84+42160dup	NM_004296.7:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X1	XM_005268231.1:c.84+42153=	XM_005268231.1:c.84+42160del	XM_005268231.1:c.84+42160dup	XM_005268231.1:c.84+42159_84+42160dup	XM_005268231.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X3	XM_005268233.1:c.84+42153=	XM_005268233.1:c.84+42160del	XM_005268233.1:c.84+42160dup	XM_005268233.1:c.84+42159_84+42160dup	XM_005268233.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X4	XM_005268234.1:c.84+42153=	XM_005268234.1:c.84+42160del	XM_005268234.1:c.84+42160dup	XM_005268234.1:c.84+42159_84+42160dup	XM_005268234.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X5	XM_005268235.1:c.84+42153=	XM_005268235.1:c.84+42160del	XM_005268235.1:c.84+42160dup	XM_005268235.1:c.84+42159_84+42160dup	XM_005268235.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X21	XM_005268236.1:c.84+42153=	XM_005268236.1:c.84+42160del	XM_005268236.1:c.84+42160dup	XM_005268236.1:c.84+42159_84+42160dup	XM_005268236.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X4	XM_017021820.3:c.84+42153=	XM_017021820.3:c.84+42160del	XM_017021820.3:c.84+42160dup	XM_017021820.3:c.84+42159_84+42160dup	XM_017021820.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X9	XM_017021822.3:c.84+42153=	XM_017021822.3:c.84+42160del	XM_017021822.3:c.84+42160dup	XM_017021822.3:c.84+42159_84+42160dup	XM_017021822.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X11	XM_017021825.3:c.84+42153=	XM_017021825.3:c.84+42160del	XM_017021825.3:c.84+42160dup	XM_017021825.3:c.84+42159_84+42160dup	XM_017021825.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X12	XM_017021826.3:c.84+42153=	XM_017021826.3:c.84+42160del	XM_017021826.3:c.84+42160dup	XM_017021826.3:c.84+42159_84+42160dup	XM_017021826.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X13	XM_017021827.3:c.84+42153=	XM_017021827.3:c.84+42160del	XM_017021827.3:c.84+42160dup	XM_017021827.3:c.84+42159_84+42160dup	XM_017021827.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X15	XM_017021828.3:c.84+42153=	XM_017021828.3:c.84+42160del	XM_017021828.3:c.84+42160dup	XM_017021828.3:c.84+42159_84+42160dup	XM_017021828.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X16	XM_017021830.3:c.84+42153=	XM_017021830.3:c.84+42160del	XM_017021830.3:c.84+42160dup	XM_017021830.3:c.84+42159_84+42160dup	XM_017021830.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X17	XM_017021831.3:c.84+42153=	XM_017021831.3:c.84+42160del	XM_017021831.3:c.84+42160dup	XM_017021831.3:c.84+42159_84+42160dup	XM_017021831.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X18	XM_017021832.3:c.84+42153=	XM_017021832.3:c.84+42160del	XM_017021832.3:c.84+42160dup	XM_017021832.3:c.84+42159_84+42160dup	XM_017021832.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X21	XM_017021833.3:c.84+42153=	XM_017021833.3:c.84+42160del	XM_017021833.3:c.84+42160dup	XM_017021833.3:c.84+42159_84+42160dup	XM_017021833.3:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X1	XM_024449759.2:c.84+42153=	XM_024449759.2:c.84+42160del	XM_024449759.2:c.84+42160dup	XM_024449759.2:c.84+42159_84+42160dup	XM_024449759.2:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X3	XM_024449760.2:c.84+42153=	XM_024449760.2:c.84+42160del	XM_024449760.2:c.84+42160dup	XM_024449760.2:c.84+42159_84+42160dup	XM_024449760.2:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X2	XM_024449761.2:c.84+42153=	XM_024449761.2:c.84+42160del	XM_024449761.2:c.84+42160dup	XM_024449761.2:c.84+42159_84+42160dup	XM_024449761.2:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X19	XM_024449776.2:c.84+42153=	XM_024449776.2:c.84+42160del	XM_024449776.2:c.84+42160dup	XM_024449776.2:c.84+42159_84+42160dup	XM_024449776.2:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X10	XM_047431987.1:c.84+42153=	XM_047431987.1:c.84+42160del	XM_047431987.1:c.84+42160dup	XM_047431987.1:c.84+42159_84+42160dup	XM_047431987.1:c.84+42160_84+42161insAAAAAAAAA
RGS6 transcript variant X20	XM_047431990.1:c.84+42153=	XM_047431990.1:c.84+42160del	XM_047431990.1:c.84+42160dup	XM_047431990.1:c.84+42159_84+42160dup	XM_047431990.1:c.84+42160_84+42161insAAAAAAAAA

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#.

43 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40485185	Mar 15, 2006 (126)
2	GMI	ss289229283	May 04, 2012 (137)
3	1000GENOMES	ss327618556	May 09, 2011 (135)
4	1000GENOMES	ss327731962	May 09, 2011 (135)
5	1000GENOMES	ss498781963	May 04, 2012 (137)
6	LUNTER	ss552373034	Apr 25, 2013 (138)
7	LUNTER	ss552704541	Apr 25, 2013 (138)
8	LUNTER	ss553554427	Apr 25, 2013 (138)
9	SSMP	ss664241259	Apr 01, 2015 (144)
10	EVA-GONL	ss991295684	Aug 21, 2014 (142)
11	1000GENOMES	ss1374260198	Aug 21, 2014 (142)
12	EVA_GENOME_DK	ss1574781591	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1708112930	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1708112999	Apr 01, 2015 (144)
15	JJLAB	ss2031237564	Sep 14, 2016 (149)
16	SWEGEN	ss3012431261	Nov 08, 2017 (151)
17	MCHAISSO	ss3063799385	Nov 08, 2017 (151)
18	BIOINF_KMB_FNS_UNIBA	ss3645354936	Oct 12, 2018 (152)
19	EGCUT_WGS	ss3679687858	Jul 13, 2019 (153)
20	EVA_DECODE	ss3696956817	Jul 13, 2019 (153)
21	EVA_DECODE	ss3696956818	Jul 13, 2019 (153)
22	EVA_DECODE	ss3696956819	Jul 13, 2019 (153)
23	ACPOP	ss3740506814	Jul 13, 2019 (153)
24	KHV_HUMAN_GENOMES	ss3817823441	Jul 13, 2019 (153)
25	EVA	ss3833991927	Apr 27, 2020 (154)
26	KOGIC	ss3975209005	Apr 27, 2020 (154)
27	GNOMAD	ss4280487236	Apr 27, 2021 (155)
28	GNOMAD	ss4280487237	Apr 27, 2021 (155)
29	GNOMAD	ss4280487238	Apr 27, 2021 (155)
30	TOPMED	ss4975546236	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5213867928	Apr 27, 2021 (155)
32	TOMMO_GENOMICS	ss5213867929	Apr 27, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5296715906	Oct 17, 2022 (156)
34	HUGCELL_USP	ss5490711167	Oct 17, 2022 (156)
35	EVA	ss5511292773	Oct 17, 2022 (156)
36	SANFORD_IMAGENETICS	ss5656499777	Oct 17, 2022 (156)
37	TOMMO_GENOMICS	ss5766854568	Oct 17, 2022 (156)
38	TOMMO_GENOMICS	ss5766854569	Oct 17, 2022 (156)
39	YY_MCH	ss5814873059	Oct 17, 2022 (156)
40	EVA	ss5841304175	Oct 17, 2022 (156)
41	EVA	ss5851093622	Oct 17, 2022 (156)
42	EVA	ss5901907853	Oct 17, 2022 (156)
43	EVA	ss5947945953	Oct 17, 2022 (156)
44	1000Genomes	NC_000014.8 - 72473745	Oct 12, 2018 (152)
45	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 72473745	Oct 12, 2018 (152)
46	Genetic variation in the Estonian population	NC_000014.8 - 72473745	Oct 12, 2018 (152)
47	The Danish reference pan genome	NC_000014.8 - 72473745	Apr 27, 2020 (154)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455263020 (NC_000014.9:72007027::A 18632/138310) Row 455263021 (NC_000014.9:72007027::AA 2/138374) Row 455263022 (NC_000014.9:72007027:A: 9/138372)	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455263020 (NC_000014.9:72007027::A 18632/138310) Row 455263021 (NC_000014.9:72007027::AA 2/138374) Row 455263022 (NC_000014.9:72007027:A: 9/138372)	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455263020 (NC_000014.9:72007027::A 18632/138310) Row 455263021 (NC_000014.9:72007027::AA 2/138374) Row 455263022 (NC_000014.9:72007027:A: 9/138372)	-	Apr 27, 2021 (155)
51	Genome of the Netherlands Release 5	NC_000014.8 - 72473745	Apr 27, 2020 (154)
52	Korean Genome Project	NC_000014.9 - 72007028	Apr 27, 2020 (154)
53	Northern Sweden	NC_000014.8 - 72473745	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 71837235 (NC_000014.8:72473744::A 2737/16760) Row 71837236 (NC_000014.8:72473744::AA 1/16760)	-	Apr 27, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 71837235 (NC_000014.8:72473744::A 2737/16760) Row 71837236 (NC_000014.8:72473744::AA 1/16760)	-	Apr 27, 2021 (155)
56	14KJPN Submission ignored due to conflicting rows: Row 100691672 (NC_000014.9:72007027::A 4512/28258) Row 100691673 (NC_000014.9:72007027::AA 1/28258)	-	Oct 17, 2022 (156)
57	14KJPN Submission ignored due to conflicting rows: Row 100691672 (NC_000014.9:72007027::A 4512/28258) Row 100691673 (NC_000014.9:72007027::AA 1/28258)	-	Oct 17, 2022 (156)
58	TopMed	NC_000014.9 - 72007028	Apr 27, 2021 (155)
59	UK 10K study - Twins	NC_000014.8 - 72473745	Oct 12, 2018 (152)
60	ALFA	NC_000014.9 - 72007028	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).

Associated ID	History Updated (Build)
rs142161066	Sep 17, 2011 (135)
rs375866736	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5511292773	NC_000014.8:72473744:A:	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAA	(self)
ss3696956819, ss4280487238	NC_000014.9:72007027:A:	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAA	(self)
13540478023	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAA	(self)
ss289229283, ss327618556, ss327731962, ss552373034, ss552704541, ss553554427	NC_000014.7:71543497::A	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
64568328, 35878713, 25426106, 459711, 16022823, 13791679, 35878713, ss498781963, ss664241259, ss991295684, ss1374260198, ss1574781591, ss1708112930, ss1708112999, ss2031237564, ss3012431261, ss3679687858, ss3740506814, ss3833991927, ss5213867928, ss5656499777, ss5841304175, ss5947945953	NC_000014.8:72473744::A	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
31587006, 191091895, ss3063799385, ss3645354936, ss3817823441, ss3975209005, ss4280487236, ss4975546236, ss5296715906, ss5490711167, ss5766854568, ss5814873059, ss5851093622, ss5901907853	NC_000014.9:72007027::A	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
13540478023	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
ss3696956818	NC_000014.9:72007028::A	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
ss40485185	NT_026437.12:53473744::A	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAA	(self)
ss5213867929	NC_000014.8:72473744::AA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAA	(self)
ss4280487237, ss5766854569	NC_000014.9:72007027::AA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAA	(self)
13540478023	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAA	(self)
13540478023	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3696956817	NC_000014.9:72007028::AAAAAAAAA	NC_000014.9:72007027:AAAAAAAA:AAAA… NC_000014.9:72007027:AAAAAAAA:AAAAAAAAAAAAAAAAA	(self)

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

No publications for rs35651129

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35651129