Name: rs1491305790
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.

rs1491305790

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:41035721-41035722 (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: dupT / insTCTTT / ins(TCTT)₂T / in…
dupT / insTCTTT / ins(TCTT)₂T / ins(TCTT)₃T / ins(TCTT)₄T / ins(TCTT)₆TTTTT / ins(TCTT)₄TTTTT / ins(TCTT)₃TTTTT / ins(TCTT)₂TTTTT / ins(TCTT)₂TTTTTT / insTC(T)₇ / ins(T)₄ / ins(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00000 (0/11862, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KRTAP1-3 : 2KB Upstream 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	11862	TT=1.00000	TTT=0.00000	1.0	N/A
European	Sub	7618	TT=1.0000	TTT=0.0000	1.0	N/A
African	Sub	2816	TT=1.0000	TTT=0.0000	1.0	N/A
African Others	Sub	108	TT=1.000	TTT=0.000	1.0	N/A
African American	Sub	2708	TT=1.0000	TTT=0.0000	1.0	N/A
Asian	Sub	108	TT=1.000	TTT=0.000	1.0	N/A
East Asian	Sub	84	TT=1.00	TTT=0.00	1.0	N/A
Other Asian	Sub	24	TT=1.00	TTT=0.00	1.0	N/A
Latin American 1	Sub	146	TT=1.000	TTT=0.000	1.0	N/A
Latin American 2	Sub	610	TT=1.000	TTT=0.000	1.0	N/A
South Asian	Sub	94	TT=1.00	TTT=0.00	1.0	N/A
Other	Sub	470	TT=1.000	TTT=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	11862	TT=1.00000	dupT=0.00000
Allele Frequency Aggregator	European	Sub	7618	TT=1.0000	dupT=0.0000
Allele Frequency Aggregator	African	Sub	2816	TT=1.0000	dupT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	TT=1.000	dupT=0.000
Allele Frequency Aggregator	Other	Sub	470	TT=1.000	dupT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	TT=1.000	dupT=0.000
Allele Frequency Aggregator	Asian	Sub	108	TT=1.000	dupT=0.000
Allele Frequency Aggregator	South Asian	Sub	94	TT=1.00	dupT=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.41035722dup
GRCh38.p14 chr 17	NC_000017.11:g.41035722_41035723insTCTTT
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[2]TTT[1]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[3]TTT[1]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[4]TTT[1]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[6]T[7]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[4]T[7]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[3]T[7]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[2]T[7]
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722TTTC[2]T[8]
GRCh38.p14 chr 17	NC_000017.11:g.41035722_41035723insTCTTTTTTT
GRCh38.p14 chr 17	NC_000017.11:g.41035722_41035723insTTTT
GRCh38.p14 chr 17	NC_000017.11:g.41035722_41035723insTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.39191974dup
GRCh37.p13 chr 17	NC_000017.10:g.39191974_39191975insTCTTT
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[2]TTT[1]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[3]TTT[1]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[4]TTT[1]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[6]T[7]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[4]T[7]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[3]T[7]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[2]T[7]
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974TTTC[2]T[8]
GRCh37.p13 chr 17	NC_000017.10:g.39191974_39191975insTCTTTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.39191974_39191975insTTTT
GRCh37.p13 chr 17	NC_000017.10:g.39191974_39191975insTTTTT
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185117dup
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185117_185118insTCTTT
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[2]TTT[1]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[3]TTT[1]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[4]TTT[1]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[6]T[7]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[4]T[7]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[3]T[7]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[2]T[7]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117TTTC[2]T[8]
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185117_185118insTCTTTTTTT
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185117_185118insTTTT
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185117_185118insTTTTT

Gene: KRTAP1-3, keratin associated protein 1-3 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
KRTAP1-3 transcript	NM_030966.2:c.	N/A	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	TT=	dupT	insTCTTT	ins(TCTT)₂T	ins(TCTT)₃T	ins(TCTT)₄T	ins(TCTT)₆TTTTT	ins(TCTT)₄TTTTT	ins(TCTT)₃TTTTT	ins(TCTT)₂TTTTT	ins(TCTT)₂TTTTTT	insTC(T)₇	ins(T)₄	ins(T)₅
GRCh38.p14 chr 17	NC_000017.11:g.41035721_41035722=	NC_000017.11:g.41035722dup	NC_000017.11:g.41035722_41035723insTCTTT	NC_000017.11:g.41035721_41035722TTTC[2]TTT[1]	NC_000017.11:g.41035721_41035722TTTC[3]TTT[1]	NC_000017.11:g.41035721_41035722TTTC[4]TTT[1]	NC_000017.11:g.41035721_41035722TTTC[6]T[7]	NC_000017.11:g.41035721_41035722TTTC[4]T[7]	NC_000017.11:g.41035721_41035722TTTC[3]T[7]	NC_000017.11:g.41035721_41035722TTTC[2]T[7]	NC_000017.11:g.41035721_41035722TTTC[2]T[8]	NC_000017.11:g.41035722_41035723insTCTTTTTTT	NC_000017.11:g.41035722_41035723insTTTT	NC_000017.11:g.41035722_41035723insTTTTT
GRCh37.p13 chr 17	NC_000017.10:g.39191973_39191974=	NC_000017.10:g.39191974dup	NC_000017.10:g.39191974_39191975insTCTTT	NC_000017.10:g.39191973_39191974TTTC[2]TTT[1]	NC_000017.10:g.39191973_39191974TTTC[3]TTT[1]	NC_000017.10:g.39191973_39191974TTTC[4]TTT[1]	NC_000017.10:g.39191973_39191974TTTC[6]T[7]	NC_000017.10:g.39191973_39191974TTTC[4]T[7]	NC_000017.10:g.39191973_39191974TTTC[3]T[7]	NC_000017.10:g.39191973_39191974TTTC[2]T[7]	NC_000017.10:g.39191973_39191974TTTC[2]T[8]	NC_000017.10:g.39191974_39191975insTCTTTTTTT	NC_000017.10:g.39191974_39191975insTTTT	NC_000017.10:g.39191974_39191975insTTTTT
GRCh38.p14 chr 17 alt locus HSCHR17_4_CTG4	NW_003871091.1:g.185116_185117=	NW_003871091.1:g.185117dup	NW_003871091.1:g.185117_185118insTCTTT	NW_003871091.1:g.185116_185117TTTC[2]TTT[1]	NW_003871091.1:g.185116_185117TTTC[3]TTT[1]	NW_003871091.1:g.185116_185117TTTC[4]TTT[1]	NW_003871091.1:g.185116_185117TTTC[6]T[7]	NW_003871091.1:g.185116_185117TTTC[4]T[7]	NW_003871091.1:g.185116_185117TTTC[3]T[7]	NW_003871091.1:g.185116_185117TTTC[2]T[7]	NW_003871091.1:g.185116_185117TTTC[2]T[8]	NW_003871091.1:g.185117_185118insTCTTTTTTT	NW_003871091.1:g.185117_185118insTTTT	NW_003871091.1:g.185117_185118insTTTTT

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#.

20 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4311398419	Apr 26, 2021 (155)
2	GNOMAD	ss4311398420	Apr 26, 2021 (155)
3	GNOMAD	ss4311398421	Apr 26, 2021 (155)
4	GNOMAD	ss4311398422	Apr 26, 2021 (155)
5	GNOMAD	ss4311398423	Apr 26, 2021 (155)
6	GNOMAD	ss4311398424	Apr 26, 2021 (155)
7	GNOMAD	ss4311398425	Apr 26, 2021 (155)
8	GNOMAD	ss4311398426	Apr 26, 2021 (155)
9	GNOMAD	ss4311398427	Apr 26, 2021 (155)
10	GNOMAD	ss4311398428	Apr 26, 2021 (155)
11	GNOMAD	ss4311398429	Apr 26, 2021 (155)
12	GNOMAD	ss4311398430	Apr 26, 2021 (155)
13	GNOMAD	ss4311398431	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5222366151	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5222366152	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5222366153	Apr 26, 2021 (155)
17	HUGCELL_USP	ss5496158792	Oct 16, 2022 (156)
18	TOMMO_GENOMICS	ss5778557557	Oct 16, 2022 (156)
19	TOMMO_GENOMICS	ss5778557558	Oct 16, 2022 (156)
20	TOMMO_GENOMICS	ss5778557559	Oct 16, 2022 (156)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 506944428 (NC_000017.11:41035720::T 22/39468) Row 506944429 (NC_000017.11:41035720::TTTCT 11/39462) Row 506944430 (NC_000017.11:41035720::TTTCTTTCT 10/39452)...	-	Apr 26, 2021 (155)
34	8.3KJPN Submission ignored due to conflicting rows: Row 80335458 (NC_000017.10:39191972::TTTTT 38/14508) Row 80335459 (NC_000017.10:39191972::TTTCTTTTT 4/14508) Row 80335460 (NC_000017.10:39191972::TTTT 1/14508)	-	Apr 26, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 80335458 (NC_000017.10:39191972::TTTTT 38/14508) Row 80335459 (NC_000017.10:39191972::TTTCTTTTT 4/14508) Row 80335460 (NC_000017.10:39191972::TTTT 1/14508)	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 80335458 (NC_000017.10:39191972::TTTTT 38/14508) Row 80335459 (NC_000017.10:39191972::TTTCTTTTT 4/14508) Row 80335460 (NC_000017.10:39191972::TTTT 1/14508)	-	Apr 26, 2021 (155)
37	14KJPN Submission ignored due to conflicting rows: Row 112394661 (NC_000017.11:41035720::TTTTT 52/20308) Row 112394662 (NC_000017.11:41035720::TTTCTTTTT 4/20308) Row 112394663 (NC_000017.11:41035720::TTTT 1/20308)	-	Oct 16, 2022 (156)
38	14KJPN Submission ignored due to conflicting rows: Row 112394661 (NC_000017.11:41035720::TTTTT 52/20308) Row 112394662 (NC_000017.11:41035720::TTTCTTTTT 4/20308) Row 112394663 (NC_000017.11:41035720::TTTT 1/20308)	-	Oct 16, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 112394661 (NC_000017.11:41035720::TTTTT 52/20308) Row 112394662 (NC_000017.11:41035720::TTTCTTTTT 4/20308) Row 112394663 (NC_000017.11:41035720::TTTT 1/20308)	-	Oct 16, 2022 (156)
40	ALFA	NC_000017.11 - 41035721	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
ss4311398419	NC_000017.11:41035720::T	NC_000017.11:41035720:TT:TTT	(self)
8582425821	NC_000017.11:41035720:TT:TTT	NC_000017.11:41035720:TT:TTT	(self)
ss4311398420	NC_000017.11:41035720::TTTCT	NC_000017.11:41035720:TT:TTTCTTT	(self)
ss4311398421	NC_000017.11:41035720::TTTCTTTCT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTT	(self)
ss4311398422	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTCT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTCTTT	(self)
ss4311398423	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTCTTTCT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTCTTTCTTT	(self)
ss4311398424	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTCTTTCTTTCTTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTCTTTCTTTCTTTCTTTTTTT	(self)
ss4311398425	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTCTTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTCTTTCTTTTTTT	(self)
ss4311398426, ss5496158792	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTCTTTTTTT	(self)
ss4311398427	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTTTTT	(self)
ss4311398428	NC_000017.11:41035720::TTTCTTTCTTT… NC_000017.11:41035720::TTTCTTTCTTTTTT	NC_000017.11:41035720:TT:TTTCTTTCT… NC_000017.11:41035720:TT:TTTCTTTCTTTTTTTT	(self)
ss5222366152	NC_000017.10:39191972::TTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTTT… NC_000017.11:41035720:TT:TTTCTTTTTTT	(self)
ss4311398429, ss5778557558	NC_000017.11:41035720::TTTCTTTTT	NC_000017.11:41035720:TT:TTTCTTTTT… NC_000017.11:41035720:TT:TTTCTTTTTTT	(self)
ss5222366153	NC_000017.10:39191972::TTTT	NC_000017.11:41035720:TT:TTTTTT	(self)
ss4311398430, ss5778557559	NC_000017.11:41035720::TTTT	NC_000017.11:41035720:TT:TTTTTT	(self)
ss5222366151	NC_000017.10:39191972::TTTTT	NC_000017.11:41035720:TT:TTTTTTT	(self)
ss4311398431, ss5778557557	NC_000017.11:41035720::TTTTT	NC_000017.11:41035720:TT:TTTTTTT	(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 rs1491305790

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

rs1491305790