Name: rs114622715
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.

rs114622715

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:726034 (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: G>A / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.007093 (995/140278, GnomAD)
A=0.00056 (8/14326, ALFA)
A=0.0101 (65/6404, 1000G_30x) (+ 5 more)
A=0.0090 (45/5008, 1000G)
A=0.002 (1/534, MGP)
A=0.009 (2/216, Qatari)
G=0.5 (1/2, SGDP_PRJ)
A=0.5 (1/2, SGDP_PRJ)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PCGF3 : Intron Variant
LOC124900172 : 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	14326	G=0.99944	A=0.00056, T=0.00000
European	Sub	9824	G=1.0000	A=0.0000, T=0.0000
African	Sub	2858	G=0.9972	A=0.0028, T=0.0000
African Others	Sub	112	G=1.000	A=0.000, T=0.000
African American	Sub	2746	G=0.9971	A=0.0029, T=0.0000
Asian	Sub	112	G=1.000	A=0.000, T=0.000
East Asian	Sub	86	G=1.00	A=0.00, T=0.00
Other Asian	Sub	26	G=1.00	A=0.00, T=0.00
Latin American 1	Sub	146	G=1.000	A=0.000, T=0.000
Latin American 2	Sub	608	G=1.000	A=0.000, T=0.000
South Asian	Sub	98	G=1.00	A=0.00, T=0.00
Other	Sub	680	G=1.000	A=0.000, T=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
gnomAD - Genomes	Global	Study-wide	140278	G=0.992907	A=0.007093
gnomAD - Genomes	European	Sub	75958	G=0.99995	A=0.00005
gnomAD - Genomes	African	Sub	42054	G=0.97748	A=0.02252
gnomAD - Genomes	American	Sub	13660	G=0.99722	A=0.00278
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=1.0000	A=0.0000
gnomAD - Genomes	East Asian	Sub	3132	G=1.0000	A=0.0000
gnomAD - Genomes	Other	Sub	2152	G=0.9972	A=0.0028
Allele Frequency Aggregator	Total	Global	14326	G=0.99944	A=0.00056, T=0.00000
Allele Frequency Aggregator	European	Sub	9824	G=1.0000	A=0.0000, T=0.0000
Allele Frequency Aggregator	African	Sub	2858	G=0.9972	A=0.0028, T=0.0000
Allele Frequency Aggregator	Other	Sub	680	G=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Latin American 2	Sub	608	G=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	G=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	Asian	Sub	112	G=1.000	A=0.000, T=0.000
Allele Frequency Aggregator	South Asian	Sub	98	G=1.00	A=0.00, T=0.00
1000Genomes_30x	Global	Study-wide	6404	G=0.9899	A=0.0101
1000Genomes_30x	African	Sub	1786	G=0.9658	A=0.0342
1000Genomes_30x	Europe	Sub	1266	G=1.0000	A=0.0000
1000Genomes_30x	South Asian	Sub	1202	G=1.0000	A=0.0000
1000Genomes_30x	East Asian	Sub	1170	G=1.0000	A=0.0000
1000Genomes_30x	American	Sub	980	G=0.996	A=0.004
1000Genomes	Global	Study-wide	5008	G=0.9910	A=0.0090
1000Genomes	African	Sub	1322	G=0.9675	A=0.0325
1000Genomes	East Asian	Sub	1008	G=1.0000	A=0.0000
1000Genomes	Europe	Sub	1006	G=1.0000	A=0.0000
1000Genomes	South Asian	Sub	978	G=1.000	A=0.000
1000Genomes	American	Sub	694	G=0.997	A=0.003
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.998	A=0.002
Qatari	Global	Study-wide	216	G=0.991	A=0.009
SGDP_PRJ	Global	Study-wide	2	G=0.5	A=0.5

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 4	NC_000004.12:g.726034G>A
GRCh38.p14 chr 4	NC_000004.12:g.726034G>T
GRCh37.p13 chr 4	NC_000004.11:g.719823G>A
GRCh37.p13 chr 4	NC_000004.11:g.719823G>T

Gene: PCGF3, polycomb group ring finger 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PCGF3 transcript variant 1	NM_001317836.3:c.-288-459… NM_001317836.3:c.-288-4596G>A	N/A	Intron Variant
PCGF3 transcript variant 3	NM_001395245.1:c.-306-459… NM_001395245.1:c.-306-4596G>A	N/A	Intron Variant
PCGF3 transcript variant 4	NM_001395246.1:c.-244-459… NM_001395246.1:c.-244-4596G>A	N/A	Intron Variant
PCGF3 transcript variant 5	NM_001395247.1:c.-289+805… NM_001395247.1:c.-289+805G>A	N/A	Intron Variant
PCGF3 transcript variant 6	NM_001395248.1:c.-245+805… NM_001395248.1:c.-245+805G>A	N/A	Intron Variant
PCGF3 transcript variant 7	NM_001395249.1:c.-190+805… NM_001395249.1:c.-190+805G>A	N/A	Intron Variant
PCGF3 transcript variant 8	NM_001395250.1:c.-432-459… NM_001395250.1:c.-432-4596G>A	N/A	Intron Variant
PCGF3 transcript variant 9	NM_001395251.1:c.-433+805… NM_001395251.1:c.-433+805G>A	N/A	Intron Variant
PCGF3 transcript variant 2	NM_006315.7:c.-189-4596G>A	N/A	Intron Variant
PCGF3 transcript variant X1	XM_047449500.1:c.	N/A	Genic Upstream Transcript Variant

Gene: LOC124900172, uncharacterized LOC124900172 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124900172 transcript	XM_047416540.1:c.747+195… XM_047416540.1:c.747+1959G>A	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	G=	A	T
GRCh38.p14 chr 4	NC_000004.12:g.726034=	NC_000004.12:g.726034G>A	NC_000004.12:g.726034G>T
GRCh37.p13 chr 4	NC_000004.11:g.719823=	NC_000004.11:g.719823G>A	NC_000004.11:g.719823G>T
PCGF3 transcript variant 1	NM_001317836.3:c.-288-4596=	NM_001317836.3:c.-288-4596G>A	NM_001317836.3:c.-288-4596G>T
PCGF3 transcript variant 3	NM_001395245.1:c.-306-4596=	NM_001395245.1:c.-306-4596G>A	NM_001395245.1:c.-306-4596G>T
PCGF3 transcript variant 4	NM_001395246.1:c.-244-4596=	NM_001395246.1:c.-244-4596G>A	NM_001395246.1:c.-244-4596G>T
PCGF3 transcript variant 5	NM_001395247.1:c.-289+805=	NM_001395247.1:c.-289+805G>A	NM_001395247.1:c.-289+805G>T
PCGF3 transcript variant 6	NM_001395248.1:c.-245+805=	NM_001395248.1:c.-245+805G>A	NM_001395248.1:c.-245+805G>T
PCGF3 transcript variant 7	NM_001395249.1:c.-190+805=	NM_001395249.1:c.-190+805G>A	NM_001395249.1:c.-190+805G>T
PCGF3 transcript variant 8	NM_001395250.1:c.-432-4596=	NM_001395250.1:c.-432-4596G>A	NM_001395250.1:c.-432-4596G>T
PCGF3 transcript variant 9	NM_001395251.1:c.-433+805=	NM_001395251.1:c.-433+805G>A	NM_001395251.1:c.-433+805G>T
PCGF3 transcript	NM_006315.4:c.-189-4596=	NM_006315.4:c.-189-4596G>A	NM_006315.4:c.-189-4596G>T
PCGF3 transcript variant 2	NM_006315.7:c.-189-4596=	NM_006315.7:c.-189-4596G>A	NM_006315.7:c.-189-4596G>T
PCGF3 transcript variant X1	XM_005272250.1:c.-244-4596=	XM_005272250.1:c.-244-4596G>A	XM_005272250.1:c.-244-4596G>T
PCGF3 transcript variant X2	XM_005272251.1:c.-189-4596=	XM_005272251.1:c.-189-4596G>A	XM_005272251.1:c.-189-4596G>T
PCGF3 transcript variant X3	XM_005272252.1:c.-189-4596=	XM_005272252.1:c.-189-4596G>A	XM_005272252.1:c.-189-4596G>T
PCGF3 transcript variant X3	XM_005272253.1:c.-1437-4596=	XM_005272253.1:c.-1437-4596G>A	XM_005272253.1:c.-1437-4596G>T
PCGF3 transcript variant X4	XM_005272254.1:c.-1338-4596=	XM_005272254.1:c.-1338-4596G>A	XM_005272254.1:c.-1338-4596G>T
PCGF3 transcript variant X6	XM_005272255.1:c.-1432-4596=	XM_005272255.1:c.-1432-4596G>A	XM_005272255.1:c.-1432-4596G>T
PCGF3 transcript variant X7	XM_005272256.1:c.-1338-4596=	XM_005272256.1:c.-1338-4596G>A	XM_005272256.1:c.-1338-4596G>T
LOC124900172 transcript	XM_047416540.1:c.*747+1959=	XM_047416540.1:c.*747+1959G>A	XM_047416540.1:c.*747+1959G>T

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#.

18 SubSNP, 9 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss220689544	Jul 14, 2010 (132)
2	TISHKOFF	ss557248901	Apr 25, 2013 (138)
3	1000GENOMES	ss1308054740	Aug 21, 2014 (142)
4	EVA_MGP	ss1711048417	Apr 01, 2015 (144)
5	WEILL_CORNELL_DGM	ss1922894383	Feb 12, 2016 (147)
6	HUMAN_LONGEVITY	ss2259754349	Dec 20, 2016 (150)
7	GNOMAD	ss2804591340	Nov 08, 2017 (151)
8	KHV_HUMAN_GENOMES	ss3804414834	Jul 13, 2019 (153)
9	SGDP_PRJ	ss3858003107	Apr 25, 2020 (154)
10	TOPMED	ss4599904078	Apr 26, 2021 (155)
11	TOPMED	ss4599904079	Apr 26, 2021 (155)
12	1000G_HIGH_COVERAGE	ss5257711417	Oct 13, 2022 (156)
13	EVA	ss5346317037	Oct 13, 2022 (156)
14	HUGCELL_USP	ss5456671520	Oct 13, 2022 (156)
15	1000G_HIGH_COVERAGE	ss5537997272	Oct 13, 2022 (156)
16	SANFORD_IMAGENETICS	ss5634156977	Oct 13, 2022 (156)
17	EVA	ss5861782500	Oct 13, 2022 (156)
18	EVA	ss5962533130	Oct 13, 2022 (156)
19	1000Genomes	NC_000004.11 - 719823	Oct 12, 2018 (152)
20	1000Genomes_30x	NC_000004.12 - 726034	Oct 13, 2022 (156)
21	gnomAD - Genomes	NC_000004.12 - 726034	Apr 26, 2021 (155)
22	Medical Genome Project healthy controls from Spanish population	NC_000004.11 - 719823	Apr 25, 2020 (154)
23	Qatari	NC_000004.11 - 719823	Apr 25, 2020 (154)
24	SGDP_PRJ	NC_000004.11 - 719823	Apr 25, 2020 (154)
25	TopMed Submission ignored due to conflicting rows: Row 437281634 (NC_000004.12:726033:G:A 2026/264690) Row 437281635 (NC_000004.12:726033:G:T 1/264690)	-	Apr 26, 2021 (155)
26	TopMed Submission ignored due to conflicting rows: Row 437281634 (NC_000004.12:726033:G:A 2026/264690) Row 437281635 (NC_000004.12:726033:G:T 1/264690)	-	Apr 26, 2021 (155)
27	ALFA	NC_000004.12 - 726034	Apr 26, 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
19391610, 164177, 4936313, 10020087, ss220689544, ss557248901, ss1308054740, ss1711048417, ss1922894383, ss2804591340, ss3858003107, ss5346317037, ss5634156977, ss5962533130	NC_000004.11:719822:G:A	NC_000004.12:726033:G:A	(self)
25523207, 137669043, 885436403, ss2259754349, ss3804414834, ss4599904078, ss5257711417, ss5456671520, ss5537997272, ss5861782500	NC_000004.12:726033:G:A	NC_000004.12:726033:G:A	(self)
885436403, ss4599904079	NC_000004.12:726033:G:T	NC_000004.12:726033:G:T	(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 rs114622715

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.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs114622715