Name: rs200984231
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.

rs200984231

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:2945838-2945846 (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 / delTT / delT / dupT / du…
del(T)₅ / delTT / delT / dupT / dupTT
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.00025 (7/28258, 14KJPN)
dupT=0.00005 (1/18412, ALFA)
dupT=0.00036 (6/16758, 8.3KJPN) (+ 2 more)
dupT=0.0056 (36/6404, 1000G_30x)
dupT=0.0002 (1/4480, Estonian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NAP1L4 : 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	HTRZ	HWEP
Total	Global	18412	TTTTTTTTT=0.99995	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.00005, TTTTTTTTTTT=0.00000	0.999891	0.000109	0
European	Sub	14076	TTTTTTTTT=0.99993	TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.00007, TTTTTTTTTTT=0.00000	0.999858	0.000142	0
African	Sub	2880	TTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	N/A
African Others	Sub	114	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	N/A
African American	Sub	2766	TTTTTTTTT=1.0000	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000	1.0	0.0	N/A
Asian	Sub	112	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	N/A
East Asian	Sub	86	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	N/A
Latin American 1	Sub	144	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	N/A
Latin American 2	Sub	606	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	N/A
South Asian	Sub	94	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00	1.0	0.0	N/A
Other	Sub	500	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000	1.0	0.0	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
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupT=0.00025
Allele Frequency Aggregator	Total	Global	18412	(T)₉=0.99995	delTT=0.00000, delT=0.00000, dupT=0.00005, dupTT=0.00000
Allele Frequency Aggregator	European	Sub	14076	(T)₉=0.99993	delTT=0.00000, delT=0.00000, dupT=0.00007, dupTT=0.00000
Allele Frequency Aggregator	African	Sub	2880	(T)₉=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	606	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	500	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	South Asian	Sub	94	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
8.3KJPN	JAPANESE	Study-wide	16758	- No frequency provided	dupT=0.00036
1000Genomes_30x	Global	Study-wide	6404	- No frequency provided	dupT=0.0056
1000Genomes_30x	African	Sub	1786	- No frequency provided	dupT=0.0039
1000Genomes_30x	Europe	Sub	1266	- No frequency provided	dupT=0.0032
1000Genomes_30x	South Asian	Sub	1202	- No frequency provided	dupT=0.0191
1000Genomes_30x	East Asian	Sub	1170	- No frequency provided	dupT=0.0000
1000Genomes_30x	American	Sub	980	- No frequency provided	dupT=0.002
Genetic variation in the Estonian population	Estonian	Study-wide	4480	- No frequency provided	dupT=0.0002

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.2945842_2945846del
GRCh38.p14 chr 11	NC_000011.10:g.2945845_2945846del
GRCh38.p14 chr 11	NC_000011.10:g.2945846del
GRCh38.p14 chr 11	NC_000011.10:g.2945846dup
GRCh38.p14 chr 11	NC_000011.10:g.2945845_2945846dup
GRCh37.p13 chr 11	NC_000011.9:g.2967072_2967076del
GRCh37.p13 chr 11	NC_000011.9:g.2967075_2967076del
GRCh37.p13 chr 11	NC_000011.9:g.2967076del
GRCh37.p13 chr 11	NC_000011.9:g.2967076dup
GRCh37.p13 chr 11	NC_000011.9:g.2967075_2967076dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176890_176894del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176893_176894del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176894del
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176894dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176893_176894dup

Gene: NAP1L4, nucleosome assembly protein 1 like 4 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NAP1L4 transcript variant 2	NM_001369375.1:c.33-196_… NM_001369375.1:c.33-196_*33-192del	N/A	Intron Variant
NAP1L4 transcript variant 3	NM_001369376.1:c.33-196_… NM_001369376.1:c.33-196_*33-192del	N/A	Intron Variant
NAP1L4 transcript variant 4	NM_001369377.1:c.33-196_… NM_001369377.1:c.33-196_*33-192del	N/A	Intron Variant
NAP1L4 transcript variant 5	NM_001369378.1:c.33-196_… NM_001369378.1:c.33-196_*33-192del	N/A	Intron Variant
NAP1L4 transcript variant 6	NM_001369379.1:c.33-196_… NM_001369379.1:c.33-196_*33-192del	N/A	Intron Variant
NAP1L4 transcript variant 7	NM_001369380.1:c.1123-196… NM_001369380.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 8	NM_001369381.1:c.1123-196… NM_001369381.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 9	NM_001369382.1:c.1123-196… NM_001369382.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 10	NM_001369383.1:c.1123-196… NM_001369383.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 11	NM_001369384.1:c.1123-196… NM_001369384.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 12	NM_001369385.1:c.1123-196… NM_001369385.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 13	NM_001369386.1:c.1123-196… NM_001369386.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 14	NM_001369388.1:c.1123-196… NM_001369388.1:c.1123-196_1123-192del	N/A	Intron Variant
NAP1L4 transcript variant 1	NM_005969.4:c.33-196_33… NM_005969.4:c.33-196_33-192del	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)₉=	del(T)₅	delTT	delT	dupT	dupTT
GRCh38.p14 chr 11	NC_000011.10:g.2945838_2945846=	NC_000011.10:g.2945842_2945846del	NC_000011.10:g.2945845_2945846del	NC_000011.10:g.2945846del	NC_000011.10:g.2945846dup	NC_000011.10:g.2945845_2945846dup
GRCh37.p13 chr 11	NC_000011.9:g.2967068_2967076=	NC_000011.9:g.2967072_2967076del	NC_000011.9:g.2967075_2967076del	NC_000011.9:g.2967076del	NC_000011.9:g.2967076dup	NC_000011.9:g.2967075_2967076dup
GRCh38.p14 chr 11 alt locus HSCHR11_1_CTG7	NT_187585.1:g.176886_176894=	NT_187585.1:g.176890_176894del	NT_187585.1:g.176893_176894del	NT_187585.1:g.176894del	NT_187585.1:g.176894dup	NT_187585.1:g.176893_176894dup
NAP1L4 transcript variant 2	NM_001369375.1:c.*33-192=	NM_001369375.1:c.33-196_33-192del	NM_001369375.1:c.33-193_33-192del	NM_001369375.1:c.*33-192del	NM_001369375.1:c.*33-192dup	NM_001369375.1:c.33-193_33-192dup
NAP1L4 transcript variant 3	NM_001369376.1:c.*33-192=	NM_001369376.1:c.33-196_33-192del	NM_001369376.1:c.33-193_33-192del	NM_001369376.1:c.*33-192del	NM_001369376.1:c.*33-192dup	NM_001369376.1:c.33-193_33-192dup
NAP1L4 transcript variant 4	NM_001369377.1:c.*33-192=	NM_001369377.1:c.33-196_33-192del	NM_001369377.1:c.33-193_33-192del	NM_001369377.1:c.*33-192del	NM_001369377.1:c.*33-192dup	NM_001369377.1:c.33-193_33-192dup
NAP1L4 transcript variant 5	NM_001369378.1:c.*33-192=	NM_001369378.1:c.33-196_33-192del	NM_001369378.1:c.33-193_33-192del	NM_001369378.1:c.*33-192del	NM_001369378.1:c.*33-192dup	NM_001369378.1:c.33-193_33-192dup
NAP1L4 transcript variant 6	NM_001369379.1:c.*33-192=	NM_001369379.1:c.33-196_33-192del	NM_001369379.1:c.33-193_33-192del	NM_001369379.1:c.*33-192del	NM_001369379.1:c.*33-192dup	NM_001369379.1:c.33-193_33-192dup
NAP1L4 transcript variant 7	NM_001369380.1:c.1123-192=	NM_001369380.1:c.1123-196_1123-192del	NM_001369380.1:c.1123-193_1123-192del	NM_001369380.1:c.1123-192del	NM_001369380.1:c.1123-192dup	NM_001369380.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 8	NM_001369381.1:c.1123-192=	NM_001369381.1:c.1123-196_1123-192del	NM_001369381.1:c.1123-193_1123-192del	NM_001369381.1:c.1123-192del	NM_001369381.1:c.1123-192dup	NM_001369381.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 9	NM_001369382.1:c.1123-192=	NM_001369382.1:c.1123-196_1123-192del	NM_001369382.1:c.1123-193_1123-192del	NM_001369382.1:c.1123-192del	NM_001369382.1:c.1123-192dup	NM_001369382.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 10	NM_001369383.1:c.1123-192=	NM_001369383.1:c.1123-196_1123-192del	NM_001369383.1:c.1123-193_1123-192del	NM_001369383.1:c.1123-192del	NM_001369383.1:c.1123-192dup	NM_001369383.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 11	NM_001369384.1:c.1123-192=	NM_001369384.1:c.1123-196_1123-192del	NM_001369384.1:c.1123-193_1123-192del	NM_001369384.1:c.1123-192del	NM_001369384.1:c.1123-192dup	NM_001369384.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 12	NM_001369385.1:c.1123-192=	NM_001369385.1:c.1123-196_1123-192del	NM_001369385.1:c.1123-193_1123-192del	NM_001369385.1:c.1123-192del	NM_001369385.1:c.1123-192dup	NM_001369385.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 13	NM_001369386.1:c.1123-192=	NM_001369386.1:c.1123-196_1123-192del	NM_001369386.1:c.1123-193_1123-192del	NM_001369386.1:c.1123-192del	NM_001369386.1:c.1123-192dup	NM_001369386.1:c.1123-193_1123-192dup
NAP1L4 transcript variant 14	NM_001369388.1:c.1123-192=	NM_001369388.1:c.1123-196_1123-192del	NM_001369388.1:c.1123-193_1123-192del	NM_001369388.1:c.1123-192del	NM_001369388.1:c.1123-192dup	NM_001369388.1:c.1123-193_1123-192dup
NAP1L4 transcript	NM_005969.3:c.*33-192=	NM_005969.3:c.33-196_33-192del	NM_005969.3:c.33-193_33-192del	NM_005969.3:c.*33-192del	NM_005969.3:c.*33-192dup	NM_005969.3:c.33-193_33-192dup
NAP1L4 transcript variant 1	NM_005969.4:c.*33-192=	NM_005969.4:c.33-196_33-192del	NM_005969.4:c.33-193_33-192del	NM_005969.4:c.*33-192del	NM_005969.4:c.*33-192dup	NM_005969.4:c.33-193_33-192dup
NAP1L4 transcript variant X1	XM_005252935.1:c.1123-192=	XM_005252935.1:c.1123-196_1123-192del	XM_005252935.1:c.1123-193_1123-192del	XM_005252935.1:c.1123-192del	XM_005252935.1:c.1123-192dup	XM_005252935.1:c.1123-193_1123-192dup
NAP1L4 transcript variant X2	XM_005252936.1:c.1123-192=	XM_005252936.1:c.1123-196_1123-192del	XM_005252936.1:c.1123-193_1123-192del	XM_005252936.1:c.1123-192del	XM_005252936.1:c.1123-192dup	XM_005252936.1:c.1123-193_1123-192dup
NAP1L4 transcript variant X3	XM_005252937.1:c.1123-192=	XM_005252937.1:c.1123-196_1123-192del	XM_005252937.1:c.1123-193_1123-192del	XM_005252937.1:c.1123-192del	XM_005252937.1:c.1123-192dup	XM_005252937.1:c.1123-193_1123-192dup
NAP1L4 transcript variant X4	XM_005252938.1:c.1123-192=	XM_005252938.1:c.1123-196_1123-192del	XM_005252938.1:c.1123-193_1123-192del	XM_005252938.1:c.1123-192del	XM_005252938.1:c.1123-192dup	XM_005252938.1:c.1123-193_1123-192dup

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#.

22 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	1000GENOMES	ss499385524	May 04, 2012 (137)
2	ILLUMINA	ss2710727682	Jan 10, 2018 (151)
3	SWEGEN	ss3007485905	Nov 08, 2017 (151)
4	EGCUT_WGS	ss3674892392	Jul 13, 2019 (153)
5	EVA_DECODE	ss3691089726	Jul 13, 2019 (153)
6	EVA_DECODE	ss3691089727	Jul 13, 2019 (153)
7	PACBIO	ss3786844936	Jul 13, 2019 (153)
8	GNOMAD	ss4229000835	Apr 26, 2021 (155)
9	GNOMAD	ss4229000836	Apr 26, 2021 (155)
10	GNOMAD	ss4229000838	Apr 26, 2021 (155)
11	GNOMAD	ss4229000839	Apr 26, 2021 (155)
12	TOPMED	ss4873086948	Apr 26, 2021 (155)
13	TOPMED	ss4873086950	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5200397268	Apr 26, 2021 (155)
15	1000G_HIGH_COVERAGE	ss5286176024	Oct 16, 2022 (156)
16	HUGCELL_USP	ss5481515226	Oct 16, 2022 (156)
17	HUGCELL_USP	ss5481515227	Oct 16, 2022 (156)
18	HUGCELL_USP	ss5481515228	Oct 16, 2022 (156)
19	1000G_HIGH_COVERAGE	ss5581189032	Oct 16, 2022 (156)
20	TOMMO_GENOMICS	ss5747071491	Oct 16, 2022 (156)
21	EVA	ss5836170543	Oct 16, 2022 (156)
22	EVA	ss5941810492	Oct 16, 2022 (156)
23	1000Genomes_30x	NC_000011.10 - 2945838	Oct 16, 2022 (156)
24	Genetic variation in the Estonian population	NC_000011.9 - 2967068	Oct 12, 2018 (152)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369580640 (NC_000011.10:2945837::T 402/139474) Row 369580641 (NC_000011.10:2945837::TT 5/139476) Row 369580643 (NC_000011.10:2945837:T: 21/139476)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369580640 (NC_000011.10:2945837::T 402/139474) Row 369580641 (NC_000011.10:2945837::TT 5/139476) Row 369580643 (NC_000011.10:2945837:T: 21/139476)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369580640 (NC_000011.10:2945837::T 402/139474) Row 369580641 (NC_000011.10:2945837::TT 5/139476) Row 369580643 (NC_000011.10:2945837:T: 21/139476)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369580640 (NC_000011.10:2945837::T 402/139474) Row 369580641 (NC_000011.10:2945837::TT 5/139476) Row 369580643 (NC_000011.10:2945837:T: 21/139476)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 369580640 (NC_000011.10:2945837::T 402/139474) Row 369580641 (NC_000011.10:2945837::TT 5/139476) Row 369580643 (NC_000011.10:2945837:T: 21/139476)...	-	Apr 26, 2021 (155)
30	8.3KJPN	NC_000011.9 - 2967068	Apr 26, 2021 (155)
31	14KJPN	NC_000011.10 - 2945838	Oct 16, 2022 (156)
32	TopMed Submission ignored due to conflicting rows: Row 88632604 (NC_000011.10:2945837::TT 9/264690) Row 88632606 (NC_000011.10:2945837:T: 40/264690)	-	Apr 26, 2021 (155)
33	TopMed Submission ignored due to conflicting rows: Row 88632604 (NC_000011.10:2945837::TT 9/264690) Row 88632606 (NC_000011.10:2945837:T: 40/264690)	-	Apr 26, 2021 (155)
34	ALFA	NC_000011.10 - 2945838	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
ss4229000839	NC_000011.10:2945837:TTTTT:	NC_000011.10:2945837:TTTTTTTTT:TTTT	(self)
ss5836170543	NC_000011.9:2967067:TT:	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTT	(self)
ss4229000838, ss5481515227	NC_000011.10:2945837:TT:	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTT	(self)
7192711918	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTT	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTT	(self)
ss3007485905, ss3786844936	NC_000011.9:2967067:T:	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTT	(self)
ss3691089726, ss4873086950, ss5481515228	NC_000011.10:2945837:T:	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTT	(self)
7192711918	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTT	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTT	(self)
20630640, 58366575, ss499385524, ss3674892392, ss5200397268, ss5941810492	NC_000011.9:2967067::T	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	(self)
ss2710727682	NC_000011.9:2967068::T	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	(self)
68714967, 80908595, ss4229000835, ss5286176024, ss5481515226, ss5581189032, ss5747071491	NC_000011.10:2945837::T	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	(self)
7192711918	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	(self)
ss3691089727	NC_000011.10:2945838::T	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTT	(self)
ss4229000836, ss4873086948	NC_000011.10:2945837::TT	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTTT	(self)
7192711918	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTTT	NC_000011.10:2945837:TTTTTTTTT:TTT… NC_000011.10:2945837:TTTTTTTTT:TTTTTTTTTTT	(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 rs200984231

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

rs200984231