Name: rs1205721262
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.

rs1205721262

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:42776664-42776682 (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 / dup(T)₅ / dup(T)₆ / dup(T)₁₂
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.00000 (0/12902, ALFA)
delT=0.00000 (0/12902, ALFA)
dupT=0.00000 (0/12902, ALFA) (+ 2 more)
dupTT=0.00000 (0/12902, ALFA)
dupTTT=0.00000 (0/12902, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: VPS25 : 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	12902	TTTTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	9218	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2330	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	86	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2244	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	104	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	80	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	138	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	588	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	80	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	444	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=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
Allele Frequency Aggregator	Total	Global	12902	(T)₁₉=1.00000	delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000
Allele Frequency Aggregator	European	Sub	9218	(T)₁₉=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	African	Sub	2330	(T)₁₉=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	588	(T)₁₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Other	Sub	444	(T)₁₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(T)₁₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Asian	Sub	104	(T)₁₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	South Asian	Sub	80	(T)₁₉=1.00	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 17	NC_000017.11:g.42776678_42776682del
GRCh38.p14 chr 17	NC_000017.11:g.42776679_42776682del
GRCh38.p14 chr 17	NC_000017.11:g.42776680_42776682del
GRCh38.p14 chr 17	NC_000017.11:g.42776681_42776682del
GRCh38.p14 chr 17	NC_000017.11:g.42776682del
GRCh38.p14 chr 17	NC_000017.11:g.42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776681_42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776680_42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776679_42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776678_42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776677_42776682dup
GRCh38.p14 chr 17	NC_000017.11:g.42776671_42776682dup
GRCh37.p13 chr 17	NC_000017.10:g.40928696_40928700del
GRCh37.p13 chr 17	NC_000017.10:g.40928697_40928700del
GRCh37.p13 chr 17	NC_000017.10:g.40928698_40928700del
GRCh37.p13 chr 17	NC_000017.10:g.40928699_40928700del
GRCh37.p13 chr 17	NC_000017.10:g.40928700del
GRCh37.p13 chr 17	NC_000017.10:g.40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928699_40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928698_40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928697_40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928696_40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928695_40928700dup
GRCh37.p13 chr 17	NC_000017.10:g.40928689_40928700dup
WNK4 RefSeqGene	NG_016227.1:g.1048_1052del
WNK4 RefSeqGene	NG_016227.1:g.1049_1052del
WNK4 RefSeqGene	NG_016227.1:g.1050_1052del
WNK4 RefSeqGene	NG_016227.1:g.1051_1052del
WNK4 RefSeqGene	NG_016227.1:g.1052del
WNK4 RefSeqGene	NG_016227.1:g.1052dup
WNK4 RefSeqGene	NG_016227.1:g.1051_1052dup
WNK4 RefSeqGene	NG_016227.1:g.1050_1052dup
WNK4 RefSeqGene	NG_016227.1:g.1049_1052dup
WNK4 RefSeqGene	NG_016227.1:g.1048_1052dup
WNK4 RefSeqGene	NG_016227.1:g.1047_1052dup
WNK4 RefSeqGene	NG_016227.1:g.1041_1052dup

Gene: VPS25, vacuolar protein sorting 25 homolog (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
VPS25 transcript	NM_032353.4:c.418+358_418… NM_032353.4:c.418+358_418+362del	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)₁₉=	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₁₂
GRCh38.p14 chr 17	NC_000017.11:g.42776664_42776682=	NC_000017.11:g.42776678_42776682del	NC_000017.11:g.42776679_42776682del	NC_000017.11:g.42776680_42776682del	NC_000017.11:g.42776681_42776682del	NC_000017.11:g.42776682del	NC_000017.11:g.42776682dup	NC_000017.11:g.42776681_42776682dup	NC_000017.11:g.42776680_42776682dup	NC_000017.11:g.42776679_42776682dup	NC_000017.11:g.42776678_42776682dup	NC_000017.11:g.42776677_42776682dup	NC_000017.11:g.42776671_42776682dup
GRCh37.p13 chr 17	NC_000017.10:g.40928682_40928700=	NC_000017.10:g.40928696_40928700del	NC_000017.10:g.40928697_40928700del	NC_000017.10:g.40928698_40928700del	NC_000017.10:g.40928699_40928700del	NC_000017.10:g.40928700del	NC_000017.10:g.40928700dup	NC_000017.10:g.40928699_40928700dup	NC_000017.10:g.40928698_40928700dup	NC_000017.10:g.40928697_40928700dup	NC_000017.10:g.40928696_40928700dup	NC_000017.10:g.40928695_40928700dup	NC_000017.10:g.40928689_40928700dup
WNK4 RefSeqGene	NG_016227.1:g.1034_1052=	NG_016227.1:g.1048_1052del	NG_016227.1:g.1049_1052del	NG_016227.1:g.1050_1052del	NG_016227.1:g.1051_1052del	NG_016227.1:g.1052del	NG_016227.1:g.1052dup	NG_016227.1:g.1051_1052dup	NG_016227.1:g.1050_1052dup	NG_016227.1:g.1049_1052dup	NG_016227.1:g.1048_1052dup	NG_016227.1:g.1047_1052dup	NG_016227.1:g.1041_1052dup
VPS25 transcript	NM_032353.3:c.418+344=	NM_032353.3:c.418+358_418+362del	NM_032353.3:c.418+359_418+362del	NM_032353.3:c.418+360_418+362del	NM_032353.3:c.418+361_418+362del	NM_032353.3:c.418+362del	NM_032353.3:c.418+362dup	NM_032353.3:c.418+361_418+362dup	NM_032353.3:c.418+360_418+362dup	NM_032353.3:c.418+359_418+362dup	NM_032353.3:c.418+358_418+362dup	NM_032353.3:c.418+357_418+362dup	NM_032353.3:c.418+351_418+362dup
VPS25 transcript	NM_032353.4:c.418+344=	NM_032353.4:c.418+358_418+362del	NM_032353.4:c.418+359_418+362del	NM_032353.4:c.418+360_418+362del	NM_032353.4:c.418+361_418+362del	NM_032353.4:c.418+362del	NM_032353.4:c.418+362dup	NM_032353.4:c.418+361_418+362dup	NM_032353.4:c.418+360_418+362dup	NM_032353.4:c.418+359_418+362dup	NM_032353.4:c.418+358_418+362dup	NM_032353.4:c.418+357_418+362dup	NM_032353.4:c.418+351_418+362dup

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#.

24 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3015537960	Nov 08, 2017 (151)
2	PACBIO	ss3793161844	Jul 13, 2019 (153)
3	GNOMAD	ss4311650040	Apr 27, 2021 (155)
4	GNOMAD	ss4311650041	Apr 27, 2021 (155)
5	GNOMAD	ss4311650042	Apr 27, 2021 (155)
6	GNOMAD	ss4311650043	Apr 27, 2021 (155)
7	GNOMAD	ss4311650044	Apr 27, 2021 (155)
8	GNOMAD	ss4311650045	Apr 27, 2021 (155)
9	GNOMAD	ss4311650046	Apr 27, 2021 (155)
10	GNOMAD	ss4311650047	Apr 27, 2021 (155)
11	GNOMAD	ss4311650048	Apr 27, 2021 (155)
12	GNOMAD	ss4311650049	Apr 27, 2021 (155)
13	GNOMAD	ss4311650050	Apr 27, 2021 (155)
14	GNOMAD	ss4311650051	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5222425558	Apr 27, 2021 (155)
16	TOMMO_GENOMICS	ss5222425559	Apr 27, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5303141206	Oct 16, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5303141207	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5303141208	Oct 16, 2022 (156)
20	HUGCELL_USP	ss5496196420	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5496196421	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5496196423	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5778636903	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5778636905	Oct 16, 2022 (156)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 507308037 (NC_000017.11:42776663::T 6023/112492) Row 507308038 (NC_000017.11:42776663::TT 120/112526) Row 507308039 (NC_000017.11:42776663::TTT 3/112546)...	-	Apr 27, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 80394865 (NC_000017.10:40928681::T 453/16732) Row 80394866 (NC_000017.10:40928681:T: 16/16732)	-	Apr 27, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 80394865 (NC_000017.10:40928681::T 453/16732) Row 80394866 (NC_000017.10:40928681:T: 16/16732)	-	Apr 27, 2021 (155)
39	14KJPN Submission ignored due to conflicting rows: Row 112474007 (NC_000017.11:42776663::T 803/28176) Row 112474009 (NC_000017.11:42776663:T: 27/28176)	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 112474007 (NC_000017.11:42776663::T 803/28176) Row 112474009 (NC_000017.11:42776663:T: 27/28176)	-	Oct 16, 2022 (156)
41	ALFA	NC_000017.11 - 42776664	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
ss4311650051	NC_000017.11:42776663:TTTTT:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4311650050	NC_000017.11:42776663:TTTT:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4311650049	NC_000017.11:42776663:TTT:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4311650048, ss5496196423	NC_000017.11:42776663:TT:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11105212972	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5222425559	NC_000017.10:40928681:T:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4311650047, ss5303141207, ss5496196420, ss5778636905	NC_000017.11:42776663:T:	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11105212972	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3015537960, ss3793161844, ss5222425558	NC_000017.10:40928681::T	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4311650040, ss5303141206, ss5496196421, ss5778636903	NC_000017.11:42776663::T	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11105212972	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4311650041, ss5303141208	NC_000017.11:42776663::TT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11105212972	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4311650042	NC_000017.11:42776663::TTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11105212972	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4311650043	NC_000017.11:42776663::TTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4311650044	NC_000017.11:42776663::TTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4311650045	NC_000017.11:42776663::TTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4311650046	NC_000017.11:42776663::TTTTTTTTTTTT	NC_000017.11:42776663:TTTTTTTTTTTT… NC_000017.11:42776663:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1205721262

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

rs1205721262