Name: rs869195749
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.

rs869195749

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:230951757-230951774 (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)₅ / del(T)₄ / delTTT / delTT…
del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: delTTT=0.000004 (1/264690, TOPMED)
del(T)₄=0.00000 (0/11364, ALFA)
delTTT=0.00000 (0/11364, ALFA) (+ 5 more)
delTT=0.00000 (0/11364, ALFA)
delT=0.00000 (0/11364, ALFA)
dupT=0.00000 (0/11364, ALFA)
dupTT=0.00000 (0/11364, ALFA)
dupTTT=0.00000 (0/11364, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GPR55 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	11364	TTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7472	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2526	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	94	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2432	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	100	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	80	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	144	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	598	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	92	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	432	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

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)₁₈=0.999996	delTTT=0.000004
Allele Frequency Aggregator	Total	Global	11364	(T)₁₈=1.00000	del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	7472	(T)₁₈=1.0000	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	2526	(T)₁₈=1.0000	del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	598	(T)₁₈=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	432	(T)₁₈=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(T)₁₈=1.000	del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	100	(T)₁₈=1.00	del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	92	(T)₁₈=1.00	del(T)₄=0.00, delTTT=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 2	NC_000002.12:g.230951770_230951774del
GRCh38.p14 chr 2	NC_000002.12:g.230951771_230951774del
GRCh38.p14 chr 2	NC_000002.12:g.230951772_230951774del
GRCh38.p14 chr 2	NC_000002.12:g.230951773_230951774del
GRCh38.p14 chr 2	NC_000002.12:g.230951774del
GRCh38.p14 chr 2	NC_000002.12:g.230951774dup
GRCh38.p14 chr 2	NC_000002.12:g.230951773_230951774dup
GRCh38.p14 chr 2	NC_000002.12:g.230951772_230951774dup
GRCh38.p14 chr 2	NC_000002.12:g.230951771_230951774dup
GRCh37.p13 chr 2	NC_000002.11:g.231816485_231816489del
GRCh37.p13 chr 2	NC_000002.11:g.231816486_231816489del
GRCh37.p13 chr 2	NC_000002.11:g.231816487_231816489del
GRCh37.p13 chr 2	NC_000002.11:g.231816488_231816489del
GRCh37.p13 chr 2	NC_000002.11:g.231816489del
GRCh37.p13 chr 2	NC_000002.11:g.231816489dup
GRCh37.p13 chr 2	NC_000002.11:g.231816488_231816489dup
GRCh37.p13 chr 2	NC_000002.11:g.231816487_231816489dup
GRCh37.p13 chr 2	NC_000002.11:g.231816486_231816489dup
GPR55 RefSeqGene	NG_050956.1:g.14467_14471del
GPR55 RefSeqGene	NG_050956.1:g.14468_14471del
GPR55 RefSeqGene	NG_050956.1:g.14469_14471del
GPR55 RefSeqGene	NG_050956.1:g.14470_14471del
GPR55 RefSeqGene	NG_050956.1:g.14471del
GPR55 RefSeqGene	NG_050956.1:g.14471dup
GPR55 RefSeqGene	NG_050956.1:g.14470_14471dup
GPR55 RefSeqGene	NG_050956.1:g.14469_14471dup
GPR55 RefSeqGene	NG_050956.1:g.14468_14471dup

Gene: GPR55, G protein-coupled receptor 55 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GPR55 transcript	NM_005683.4:c.	N/A	Genic Upstream Transcript Variant
GPR55 transcript variant X2	XM_011512175.4:c.-135+901… XM_011512175.4:c.-135+9014_-135+9018del	N/A	Intron Variant
GPR55 transcript variant X1	XM_005246952.5:c.	N/A	Genic Upstream Transcript Variant
GPR55 transcript variant X3	XM_011512176.3: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	(T)₁₈=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 2	NC_000002.12:g.230951757_230951774=	NC_000002.12:g.230951770_230951774del	NC_000002.12:g.230951771_230951774del	NC_000002.12:g.230951772_230951774del	NC_000002.12:g.230951773_230951774del	NC_000002.12:g.230951774del	NC_000002.12:g.230951774dup	NC_000002.12:g.230951773_230951774dup	NC_000002.12:g.230951772_230951774dup	NC_000002.12:g.230951771_230951774dup
GRCh37.p13 chr 2	NC_000002.11:g.231816472_231816489=	NC_000002.11:g.231816485_231816489del	NC_000002.11:g.231816486_231816489del	NC_000002.11:g.231816487_231816489del	NC_000002.11:g.231816488_231816489del	NC_000002.11:g.231816489del	NC_000002.11:g.231816489dup	NC_000002.11:g.231816488_231816489dup	NC_000002.11:g.231816487_231816489dup	NC_000002.11:g.231816486_231816489dup
GPR55 RefSeqGene	NG_050956.1:g.14454_14471=	NG_050956.1:g.14467_14471del	NG_050956.1:g.14468_14471del	NG_050956.1:g.14469_14471del	NG_050956.1:g.14470_14471del	NG_050956.1:g.14471del	NG_050956.1:g.14471dup	NG_050956.1:g.14470_14471dup	NG_050956.1:g.14469_14471dup	NG_050956.1:g.14468_14471dup
GPR55 transcript variant X2	XM_011512175.4:c.-135+9018=	XM_011512175.4:c.-135+9014_-135+9018del	XM_011512175.4:c.-135+9015_-135+9018del	XM_011512175.4:c.-135+9016_-135+9018del	XM_011512175.4:c.-135+9017_-135+9018del	XM_011512175.4:c.-135+9018del	XM_011512175.4:c.-135+9018dup	XM_011512175.4:c.-135+9017_-135+9018dup	XM_011512175.4:c.-135+9016_-135+9018dup	XM_011512175.4:c.-135+9015_-135+9018dup

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#.

27 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193594808	Mar 15, 2016 (147)
2	SYSTEMSBIOZJU	ss2625102759	Nov 08, 2017 (151)
3	EVA_DECODE	ss3706225135	Jul 13, 2019 (153)
4	EVA_DECODE	ss3706225136	Jul 13, 2019 (153)
5	EVA_DECODE	ss3706225137	Jul 13, 2019 (153)
6	EVA_DECODE	ss3706225138	Jul 13, 2019 (153)
7	KOGIC	ss3950286395	Apr 25, 2020 (154)
8	KOGIC	ss3950286396	Apr 25, 2020 (154)
9	KOGIC	ss3950286397	Apr 25, 2020 (154)
10	GNOMAD	ss4062840703	Apr 26, 2021 (155)
11	GNOMAD	ss4062840704	Apr 26, 2021 (155)
12	GNOMAD	ss4062840705	Apr 26, 2021 (155)
13	GNOMAD	ss4062840706	Apr 26, 2021 (155)
14	GNOMAD	ss4062840708	Apr 26, 2021 (155)
15	GNOMAD	ss4062840709	Apr 26, 2021 (155)
16	GNOMAD	ss4062840710	Apr 26, 2021 (155)
17	TOPMED	ss4548147291	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5156953237	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5156953238	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5156953239	Apr 26, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5252386580	Oct 13, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5252386582	Oct 13, 2022 (156)
23	HUGCELL_USP	ss5451966531	Oct 13, 2022 (156)
24	HUGCELL_USP	ss5451966533	Oct 13, 2022 (156)
25	TOMMO_GENOMICS	ss5687970454	Oct 13, 2022 (156)
26	TOMMO_GENOMICS	ss5687970455	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5687970457	Oct 13, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 93852695 (NC_000002.12:230951756::T 2418/43600) Row 93852696 (NC_000002.12:230951756::TT 49/43642) Row 93852697 (NC_000002.12:230951756::TTT 7/43650)...	-	Apr 26, 2021 (155)
36	Korean Genome Project Submission ignored due to conflicting rows: Row 6664396 (NC_000002.12:230951757:TT: 6/1828) Row 6664397 (NC_000002.12:230951759::T 48/1828) Row 6664398 (NC_000002.12:230951758:T: 50/1828)	-	Apr 25, 2020 (154)
37	Korean Genome Project Submission ignored due to conflicting rows: Row 6664396 (NC_000002.12:230951757:TT: 6/1828) Row 6664397 (NC_000002.12:230951759::T 48/1828) Row 6664398 (NC_000002.12:230951758:T: 50/1828)	-	Apr 25, 2020 (154)
38	Korean Genome Project Submission ignored due to conflicting rows: Row 6664396 (NC_000002.12:230951757:TT: 6/1828) Row 6664397 (NC_000002.12:230951759::T 48/1828) Row 6664398 (NC_000002.12:230951758:T: 50/1828)	-	Apr 25, 2020 (154)
39	8.3KJPN Submission ignored due to conflicting rows: Row 14922544 (NC_000002.11:231816471:T: 253/16746) Row 14922545 (NC_000002.11:231816471::T 335/16746) Row 14922546 (NC_000002.11:231816471::TT 1/16746)	-	Apr 26, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 14922544 (NC_000002.11:231816471:T: 253/16746) Row 14922545 (NC_000002.11:231816471::T 335/16746) Row 14922546 (NC_000002.11:231816471::TT 1/16746)	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 14922544 (NC_000002.11:231816471:T: 253/16746) Row 14922545 (NC_000002.11:231816471::T 335/16746) Row 14922546 (NC_000002.11:231816471::TT 1/16746)	-	Apr 26, 2021 (155)
42	14KJPN Submission ignored due to conflicting rows: Row 21807558 (NC_000002.12:230951756::T 550/28194) Row 21807559 (NC_000002.12:230951756:T: 393/28194) Row 21807561 (NC_000002.12:230951756::TT 1/28194)	-	Oct 13, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 21807558 (NC_000002.12:230951756::T 550/28194) Row 21807559 (NC_000002.12:230951756:T: 393/28194) Row 21807561 (NC_000002.12:230951756::TT 1/28194)	-	Oct 13, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 21807558 (NC_000002.12:230951756::T 550/28194) Row 21807559 (NC_000002.12:230951756:T: 393/28194) Row 21807561 (NC_000002.12:230951756::TT 1/28194)	-	Oct 13, 2022 (156)
45	TopMed	NC_000002.12 - 230951757	Apr 26, 2021 (155)
46	ALFA	NC_000002.12 - 230951757	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
ss3706225135	NC_000002.12:230951756:TTTTT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4062840710	NC_000002.12:230951756:TTTT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
351970170, ss4062840709, ss4548147291	NC_000002.12:230951756:TTT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss2625102759	NC_000002.11:231816471:TT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4062840708	NC_000002.12:230951756:TT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3950286395	NC_000002.12:230951757:TT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3706225136	NC_000002.12:230951759:TT:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5156953237	NC_000002.11:231816471:T:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5252386582, ss5451966531, ss5687970455	NC_000002.12:230951756:T:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3950286397	NC_000002.12:230951758:T:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3706225137	NC_000002.12:230951760:T:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss193594808	NT_005403.17:82025889:T:	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5156953238	NC_000002.11:231816471::T	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4062840703, ss5252386580, ss5451966533, ss5687970454	NC_000002.12:230951756::T	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3950286396	NC_000002.12:230951759::T	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3706225138	NC_000002.12:230951761::T	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5156953239	NC_000002.11:231816471::TT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4062840704, ss5687970457	NC_000002.12:230951756::TT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4062840705	NC_000002.12:230951756::TTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
1748310923	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4062840706	NC_000002.12:230951756::TTTT	NC_000002.12:230951756:TTTTTTTTTTT… NC_000002.12:230951756:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(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 rs869195749

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

rs869195749