Name: rs200701601
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.

rs200701601

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:76782564-76782578 (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)₄ / delTTT / delTT / delT / …
del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.05110 (597/11682, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TSKU : Intron Variant
TSKU-AS1 : 500B Downstream 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	Alt HMOZ	HTRZ	HWEP
Total	Global	11682	TTTTTTTTTTTTTTT=0.94847	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00017, TTTTTTTTTTTTTTTT=0.05110, TTTTTTTTTTTTTTTTT=0.00026, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000	0.912783	0.015079	0.072138	32
European	Sub	9616	TTTTTTTTTTTTTTT=0.9375	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTT=0.0620, TTTTTTTTTTTTTTTTT=0.0003, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	0.894233	0.018322	0.087445	32
African	Sub	1228	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	54	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1174	TTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	24	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	22	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTT=1.0	TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	92	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	428	TTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	244	TTTTTTTTTTTTTTT=0.996	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000	0.991803	0.0	0.008197	0

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	11682	(T)₁₅=0.94847	delTTT=0.00000, delTT=0.00000, delT=0.00017, dupT=0.05110, dupTT=0.00026, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	9616	(T)₁₅=0.9375	delTTT=0.0000, delTT=0.0000, delT=0.0002, dupT=0.0620, dupTT=0.0003, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	1228	(T)₁₅=1.0000	delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	428	(T)₁₅=1.000	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	244	(T)₁₅=0.996	delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.004, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	92	(T)₁₅=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₁₅=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	24	(T)₁₅=1.00	delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=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 11	NC_000011.10:g.76782575_76782578del
GRCh38.p14 chr 11	NC_000011.10:g.76782576_76782578del
GRCh38.p14 chr 11	NC_000011.10:g.76782577_76782578del
GRCh38.p14 chr 11	NC_000011.10:g.76782578del
GRCh38.p14 chr 11	NC_000011.10:g.76782578dup
GRCh38.p14 chr 11	NC_000011.10:g.76782577_76782578dup
GRCh38.p14 chr 11	NC_000011.10:g.76782576_76782578dup
GRCh38.p14 chr 11	NC_000011.10:g.76782575_76782578dup
GRCh37.p13 chr 11	NC_000011.9:g.76493619_76493622del
GRCh37.p13 chr 11	NC_000011.9:g.76493620_76493622del
GRCh37.p13 chr 11	NC_000011.9:g.76493621_76493622del
GRCh37.p13 chr 11	NC_000011.9:g.76493622del
GRCh37.p13 chr 11	NC_000011.9:g.76493622dup
GRCh37.p13 chr 11	NC_000011.9:g.76493621_76493622dup
GRCh37.p13 chr 11	NC_000011.9:g.76493620_76493622dup
GRCh37.p13 chr 11	NC_000011.9:g.76493619_76493622dup

Gene: TSKU, tsukushi, small leucine rich proteoglycan (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TSKU transcript variant 2	NM_001258210.2:c.-9+142_-… NM_001258210.2:c.-9+142_-9+145del	N/A	Intron Variant
TSKU transcript variant 3	NM_001318477.2:c.	N/A	Genic Upstream Transcript Variant
TSKU transcript variant 4	NM_001318478.2:c.	N/A	Genic Upstream Transcript Variant
TSKU transcript variant 5	NM_001318479.2:c.	N/A	Genic Upstream Transcript Variant
TSKU transcript variant 1	NM_015516.4:c.	N/A	Genic Upstream Transcript Variant
TSKU transcript variant X1	XM_047426726.1:c.	N/A	Genic Upstream Transcript Variant

Gene: TSKU-AS1, TSKU antisense RNA 1 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TSKU-AS1 transcript variant 1	NR_120561.1:n.	N/A	Downstream Transcript Variant
TSKU-AS1 transcript variant 2	NR_120562.1:n.	N/A	Downstream 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)₁₅=	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 11	NC_000011.10:g.76782564_76782578=	NC_000011.10:g.76782575_76782578del	NC_000011.10:g.76782576_76782578del	NC_000011.10:g.76782577_76782578del	NC_000011.10:g.76782578del	NC_000011.10:g.76782578dup	NC_000011.10:g.76782577_76782578dup	NC_000011.10:g.76782576_76782578dup	NC_000011.10:g.76782575_76782578dup
GRCh37.p13 chr 11	NC_000011.9:g.76493608_76493622=	NC_000011.9:g.76493619_76493622del	NC_000011.9:g.76493620_76493622del	NC_000011.9:g.76493621_76493622del	NC_000011.9:g.76493622del	NC_000011.9:g.76493622dup	NC_000011.9:g.76493621_76493622dup	NC_000011.9:g.76493620_76493622dup	NC_000011.9:g.76493619_76493622dup
TSKU transcript variant 2	NM_001258210.1:c.-9+131=	NM_001258210.1:c.-9+142_-9+145del	NM_001258210.1:c.-9+143_-9+145del	NM_001258210.1:c.-9+144_-9+145del	NM_001258210.1:c.-9+145del	NM_001258210.1:c.-9+145dup	NM_001258210.1:c.-9+144_-9+145dup	NM_001258210.1:c.-9+143_-9+145dup	NM_001258210.1:c.-9+142_-9+145dup
TSKU transcript variant 2	NM_001258210.2:c.-9+131=	NM_001258210.2:c.-9+142_-9+145del	NM_001258210.2:c.-9+143_-9+145del	NM_001258210.2:c.-9+144_-9+145del	NM_001258210.2:c.-9+145del	NM_001258210.2:c.-9+145dup	NM_001258210.2:c.-9+144_-9+145dup	NM_001258210.2:c.-9+143_-9+145dup	NM_001258210.2:c.-9+142_-9+145dup

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#.

38 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss289081381	May 04, 2012 (137)
2	SSMP	ss664069616	Apr 01, 2015 (144)
3	SWEGEN	ss3008374581	Nov 08, 2017 (151)
4	MCHAISSO	ss3063698251	Nov 08, 2017 (151)
5	EVA_DECODE	ss3692117326	Jul 13, 2019 (153)
6	EVA_DECODE	ss3692117327	Jul 13, 2019 (153)
7	EVA_DECODE	ss3692117328	Jul 13, 2019 (153)
8	EVA_DECODE	ss3692117329	Jul 13, 2019 (153)
9	EVA_DECODE	ss3692117330	Jul 13, 2019 (153)
10	PACBIO	ss3786996233	Jul 13, 2019 (153)
11	EVA	ss3832709037	Apr 26, 2020 (154)
12	EVA	ss3839913307	Apr 26, 2020 (154)
13	EVA	ss3845393585	Apr 26, 2020 (154)
14	GNOMAD	ss4238128698	Apr 26, 2021 (155)
15	GNOMAD	ss4238128699	Apr 26, 2021 (155)
16	GNOMAD	ss4238128700	Apr 26, 2021 (155)
17	GNOMAD	ss4238128701	Apr 26, 2021 (155)
18	GNOMAD	ss4238128703	Apr 26, 2021 (155)
19	GNOMAD	ss4238128704	Apr 26, 2021 (155)
20	GNOMAD	ss4238128705	Apr 26, 2021 (155)
21	GNOMAD	ss4238128706	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5202772541	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5202772542	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5202772543	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5202772544	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5288025983	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5288025984	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5288025985	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5288025986	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5483120952	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5483120953	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5483120954	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5483120955	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5483120956	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5750904977	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5750904978	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5750904979	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5750904980	Oct 16, 2022 (156)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384704350 (NC_000011.10:76782563::T 23579/131576) Row 384704351 (NC_000011.10:76782563::TT 4626/131616) Row 384704352 (NC_000011.10:76782563::TTT 274/131644)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 60741848 (NC_000011.9:76493607::T 6646/16680) Row 60741849 (NC_000011.9:76493607:T: 516/16680) Row 60741850 (NC_000011.9:76493607::TT 25/16680)...	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 60741848 (NC_000011.9:76493607::T 6646/16680) Row 60741849 (NC_000011.9:76493607:T: 516/16680) Row 60741850 (NC_000011.9:76493607::TT 25/16680)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 60741848 (NC_000011.9:76493607::T 6646/16680) Row 60741849 (NC_000011.9:76493607:T: 516/16680) Row 60741850 (NC_000011.9:76493607::TT 25/16680)...	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 60741848 (NC_000011.9:76493607::T 6646/16680) Row 60741849 (NC_000011.9:76493607:T: 516/16680) Row 60741850 (NC_000011.9:76493607::TT 25/16680)...	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 84742081 (NC_000011.10:76782563::T 11611/28256) Row 84742082 (NC_000011.10:76782563:T: 871/28256) Row 84742083 (NC_000011.10:76782563::TT 42/28256)...	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 84742081 (NC_000011.10:76782563::T 11611/28256) Row 84742082 (NC_000011.10:76782563:T: 871/28256) Row 84742083 (NC_000011.10:76782563::TT 42/28256)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 84742081 (NC_000011.10:76782563::T 11611/28256) Row 84742082 (NC_000011.10:76782563:T: 871/28256) Row 84742083 (NC_000011.10:76782563::TT 42/28256)...	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 84742081 (NC_000011.10:76782563::T 11611/28256) Row 84742082 (NC_000011.10:76782563:T: 871/28256) Row 84742083 (NC_000011.10:76782563::TT 42/28256)...	-	Oct 16, 2022 (156)
55	ALFA	NC_000011.10 - 76782564	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).

Associated ID	History Updated (Build)
rs369187713	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4238128706	NC_000011.10:76782563:TTTT:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3692117326, ss4238128705	NC_000011.10:76782563:TTT:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5202772544	NC_000011.9:76493607:TT:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4238128704, ss5483120954, ss5750904980	NC_000011.10:76782563:TT:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3692117327	NC_000011.10:76782564:TT:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3008374581, ss3786996233, ss5202772542	NC_000011.9:76493607:T:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4238128703, ss5288025986, ss5483120952, ss5750904978	NC_000011.10:76782563:T:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3692117328	NC_000011.10:76782565:T:	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss289081381	NC_000011.8:76171270::T	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss664069616, ss3832709037, ss3839913307, ss5202772541	NC_000011.9:76493607::T	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3063698251, ss3845393585, ss4238128698, ss5288025983, ss5483120953, ss5750904977	NC_000011.10:76782563::T	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3692117329	NC_000011.10:76782566::T	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5202772543	NC_000011.9:76493607::TT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4238128699, ss5288025985, ss5483120955, ss5750904979	NC_000011.10:76782563::TT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3692117330	NC_000011.10:76782566::TT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4238128700, ss5288025984, ss5483120956	NC_000011.10:76782563::TTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4238128701	NC_000011.10:76782563::TTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4274002177	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:76782563:TTTTTTTTTTTT… NC_000011.10:76782563:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(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 rs200701601

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

rs200701601