Name: rs796843812
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.

rs796843812

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:67855888-67855898 (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: delGG / delG / dupG / dupGG / dupG…
delGG / delG / dupG / dupGG / dupGGG / dup(G)₄ / dup(G)₅
Variation Type: Indel Insertion and Deletion
Frequency: delGG=0.0000 (0/9916, ALFA)
delG=0.0000 (0/9916, ALFA)
dupG=0.0000 (0/9916, ALFA) (+ 4 more)
dupGG=0.0000 (0/9916, ALFA)
dupGGG=0.0000 (0/9916, ALFA)
dup(G)₄=0.0000 (0/9916, ALFA)
dup(G)₅=0.0000 (0/9916, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NUTF2 : 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	9916	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	6644	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	2086	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	62	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	2024	GGGGGGGGGGG=1.0000	GGGGGGGGG=0.0000, GGGGGGGGGG=0.0000, GGGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	102	GGGGGGGGGGG=1.000	GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000	1.0	N/A
East Asian	Sub	80	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	22	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	120	GGGGGGGGGGG=1.000	GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000	1.0	N/A
Latin American 2	Sub	484	GGGGGGGGGGG=1.000	GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	84	GGGGGGGGGGG=1.00	GGGGGGGGG=0.00, GGGGGGGGGG=0.00, GGGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	396	GGGGGGGGGGG=1.000	GGGGGGGGG=0.000, GGGGGGGGGG=0.000, GGGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGGG=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9916	(G)₁₁=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	European	Sub	6644	(G)₁₁=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	African	Sub	2086	(G)₁₁=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000, dup(G)₄=0.0000, dup(G)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	484	(G)₁₁=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Other	Sub	396	(G)₁₁=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	120	(G)₁₁=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	Asian	Sub	102	(G)₁₁=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000, dup(G)₄=0.000, dup(G)₅=0.000
Allele Frequency Aggregator	South Asian	Sub	84	(G)₁₁=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00, dup(G)₄=0.00, dup(G)₅=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 16	NC_000016.10:g.67855897_67855898del
GRCh38.p14 chr 16	NC_000016.10:g.67855898del
GRCh38.p14 chr 16	NC_000016.10:g.67855898dup
GRCh38.p14 chr 16	NC_000016.10:g.67855897_67855898dup
GRCh38.p14 chr 16	NC_000016.10:g.67855896_67855898dup
GRCh38.p14 chr 16	NC_000016.10:g.67855895_67855898dup
GRCh38.p14 chr 16	NC_000016.10:g.67855894_67855898dup
GRCh37.p13 chr 16	NC_000016.9:g.67889800_67889801del
GRCh37.p13 chr 16	NC_000016.9:g.67889801del
GRCh37.p13 chr 16	NC_000016.9:g.67889801dup
GRCh37.p13 chr 16	NC_000016.9:g.67889800_67889801dup
GRCh37.p13 chr 16	NC_000016.9:g.67889799_67889801dup
GRCh37.p13 chr 16	NC_000016.9:g.67889798_67889801dup
GRCh37.p13 chr 16	NC_000016.9:g.67889797_67889801dup

Gene: NUTF2, nuclear transport factor 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUTF2 transcript variant 2	NM_001322038.2:c.-119-456… NM_001322038.2:c.-119-4564_-119-4563del	N/A	Intron Variant
NUTF2 transcript variant 3	NM_001322039.2:c.-30+8441… NM_001322039.2:c.-30+8441_-30+8442del	N/A	Intron Variant
NUTF2 transcript variant 4	NM_001322040.2:c.-30+8441… NM_001322040.2:c.-30+8441_-30+8442del	N/A	Intron Variant
NUTF2 transcript variant 5	NM_001322041.2:c.-30+8331… NM_001322041.2:c.-30+8331_-30+8332del	N/A	Intron Variant
NUTF2 transcript variant 1	NM_005796.3:c.-30+8912_-3… NM_005796.3:c.-30+8912_-30+8913del	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	(G)₁₁=	delGG	delG	dupG	dupGG	dupGGG	dup(G)₄	dup(G)₅
GRCh38.p14 chr 16	NC_000016.10:g.67855888_67855898=	NC_000016.10:g.67855897_67855898del	NC_000016.10:g.67855898del	NC_000016.10:g.67855898dup	NC_000016.10:g.67855897_67855898dup	NC_000016.10:g.67855896_67855898dup	NC_000016.10:g.67855895_67855898dup	NC_000016.10:g.67855894_67855898dup
GRCh37.p13 chr 16	NC_000016.9:g.67889791_67889801=	NC_000016.9:g.67889800_67889801del	NC_000016.9:g.67889801del	NC_000016.9:g.67889801dup	NC_000016.9:g.67889800_67889801dup	NC_000016.9:g.67889799_67889801dup	NC_000016.9:g.67889798_67889801dup	NC_000016.9:g.67889797_67889801dup
NUTF2 transcript variant 2	NM_001322038.2:c.-119-4573=	NM_001322038.2:c.-119-4564_-119-4563del	NM_001322038.2:c.-119-4563del	NM_001322038.2:c.-119-4563dup	NM_001322038.2:c.-119-4564_-119-4563dup	NM_001322038.2:c.-119-4565_-119-4563dup	NM_001322038.2:c.-119-4566_-119-4563dup	NM_001322038.2:c.-119-4567_-119-4563dup
NUTF2 transcript variant 3	NM_001322039.2:c.-30+8432=	NM_001322039.2:c.-30+8441_-30+8442del	NM_001322039.2:c.-30+8442del	NM_001322039.2:c.-30+8442dup	NM_001322039.2:c.-30+8441_-30+8442dup	NM_001322039.2:c.-30+8440_-30+8442dup	NM_001322039.2:c.-30+8439_-30+8442dup	NM_001322039.2:c.-30+8438_-30+8442dup
NUTF2 transcript variant 4	NM_001322040.2:c.-30+8432=	NM_001322040.2:c.-30+8441_-30+8442del	NM_001322040.2:c.-30+8442del	NM_001322040.2:c.-30+8442dup	NM_001322040.2:c.-30+8441_-30+8442dup	NM_001322040.2:c.-30+8440_-30+8442dup	NM_001322040.2:c.-30+8439_-30+8442dup	NM_001322040.2:c.-30+8438_-30+8442dup
NUTF2 transcript variant 5	NM_001322041.2:c.-30+8322=	NM_001322041.2:c.-30+8331_-30+8332del	NM_001322041.2:c.-30+8332del	NM_001322041.2:c.-30+8332dup	NM_001322041.2:c.-30+8331_-30+8332dup	NM_001322041.2:c.-30+8330_-30+8332dup	NM_001322041.2:c.-30+8329_-30+8332dup	NM_001322041.2:c.-30+8328_-30+8332dup
NUTF2 transcript	NM_005796.1:c.-30+8903=	NM_005796.1:c.-30+8912_-30+8913del	NM_005796.1:c.-30+8913del	NM_005796.1:c.-30+8913dup	NM_005796.1:c.-30+8912_-30+8913dup	NM_005796.1:c.-30+8911_-30+8913dup	NM_005796.1:c.-30+8910_-30+8913dup	NM_005796.1:c.-30+8909_-30+8913dup
NUTF2 transcript variant 1	NM_005796.3:c.-30+8903=	NM_005796.3:c.-30+8912_-30+8913del	NM_005796.3:c.-30+8913del	NM_005796.3:c.-30+8913dup	NM_005796.3:c.-30+8912_-30+8913dup	NM_005796.3:c.-30+8911_-30+8913dup	NM_005796.3:c.-30+8910_-30+8913dup	NM_005796.3:c.-30+8909_-30+8913dup
NUTF2 transcript variant X1	XM_005255771.1:c.-30+8432=	XM_005255771.1:c.-30+8441_-30+8442del	XM_005255771.1:c.-30+8442del	XM_005255771.1:c.-30+8442dup	XM_005255771.1:c.-30+8441_-30+8442dup	XM_005255771.1:c.-30+8440_-30+8442dup	XM_005255771.1:c.-30+8439_-30+8442dup	XM_005255771.1:c.-30+8438_-30+8442dup

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#.

26 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80338546	Oct 12, 2018 (152)
2	HGSV	ss82308770	Oct 12, 2018 (152)
3	HAMMER_LAB	ss1808561631	Sep 08, 2015 (146)
4	SWEGEN	ss3014694661	Nov 08, 2017 (151)
5	ACPOP	ss3741608586	Jul 13, 2019 (153)
6	ACPOP	ss3741608587	Jul 13, 2019 (153)
7	INMEGENXS	ss3745616467	Jul 13, 2019 (153)
8	EVA	ss3834625750	Apr 27, 2020 (154)
9	GNOMAD	ss4302984020	Apr 27, 2021 (155)
10	GNOMAD	ss4302984021	Apr 27, 2021 (155)
11	GNOMAD	ss4302984022	Apr 27, 2021 (155)
12	GNOMAD	ss4302984023	Apr 27, 2021 (155)
13	GNOMAD	ss4302984025	Apr 27, 2021 (155)
14	GNOMAD	ss4302984026	Apr 27, 2021 (155)
15	TOMMO_GENOMICS	ss5220088686	Apr 27, 2021 (155)
16	TOMMO_GENOMICS	ss5220088687	Apr 27, 2021 (155)
17	TOMMO_GENOMICS	ss5220088688	Apr 27, 2021 (155)
18	1000G_HIGH_COVERAGE	ss5301351866	Oct 17, 2022 (156)
19	HUGCELL_USP	ss5494666941	Oct 17, 2022 (156)
20	HUGCELL_USP	ss5494666942	Oct 17, 2022 (156)
21	HUGCELL_USP	ss5494666943	Oct 17, 2022 (156)
22	SANFORD_IMAGENETICS	ss5659123821	Oct 17, 2022 (156)
23	TOMMO_GENOMICS	ss5775246880	Oct 17, 2022 (156)
24	TOMMO_GENOMICS	ss5775246881	Oct 17, 2022 (156)
25	TOMMO_GENOMICS	ss5775246882	Oct 17, 2022 (156)
26	EVA	ss5851613124	Oct 17, 2022 (156)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 492870758 (NC_000016.10:67855887::G 2846/31746) Row 492870759 (NC_000016.10:67855887::GG 1039/31810) Row 492870760 (NC_000016.10:67855887::GGG 102/31982)...	-	Apr 27, 2021 (155)
33	Northern Sweden Submission ignored due to conflicting rows: Row 14893451 (NC_000016.9:67889790::G 7/482) Row 14893452 (NC_000016.9:67889790:G: 3/482)	-	Jul 13, 2019 (153)
34	Northern Sweden Submission ignored due to conflicting rows: Row 14893451 (NC_000016.9:67889790::G 7/482) Row 14893452 (NC_000016.9:67889790:G: 3/482)	-	Jul 13, 2019 (153)
35	8.3KJPN Submission ignored due to conflicting rows: Row 78057993 (NC_000016.9:67889790:G: 55/15924) Row 78057994 (NC_000016.9:67889790::G 315/15924) Row 78057995 (NC_000016.9:67889790::GG 3/15924)	-	Apr 27, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 78057993 (NC_000016.9:67889790:G: 55/15924) Row 78057994 (NC_000016.9:67889790::G 315/15924) Row 78057995 (NC_000016.9:67889790::GG 3/15924)	-	Apr 27, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 78057993 (NC_000016.9:67889790:G: 55/15924) Row 78057994 (NC_000016.9:67889790::G 315/15924) Row 78057995 (NC_000016.9:67889790::GG 3/15924)	-	Apr 27, 2021 (155)
38	14KJPN Submission ignored due to conflicting rows: Row 109083984 (NC_000016.10:67855887:G: 86/26986) Row 109083985 (NC_000016.10:67855887::G 568/26986) Row 109083986 (NC_000016.10:67855887::GG 3/26986)	-	Oct 17, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 109083984 (NC_000016.10:67855887:G: 86/26986) Row 109083985 (NC_000016.10:67855887::G 568/26986) Row 109083986 (NC_000016.10:67855887::GG 3/26986)	-	Oct 17, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 109083984 (NC_000016.10:67855887:G: 86/26986) Row 109083985 (NC_000016.10:67855887::G 568/26986) Row 109083986 (NC_000016.10:67855887::GG 3/26986)	-	Oct 17, 2022 (156)
41	ALFA	NC_000016.10 - 67855888	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
ss4302984026	NC_000016.10:67855887:GG:	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGG	(self)
ss3014694661, ss3741608587, ss5220088686, ss5659123821	NC_000016.9:67889790:G:	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss4302984025, ss5494666942, ss5775246880, ss5851613124	NC_000016.10:67855887:G:	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGG	(self)
ss1808561631, ss3741608586, ss3745616467, ss5220088687	NC_000016.9:67889790::G	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss4302984020, ss5301351866, ss5494666941, ss5775246881	NC_000016.10:67855887::G	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGG	(self)
ss3834625750, ss5220088688	NC_000016.9:67889790::GG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4302984021, ss5494666943, ss5775246882	NC_000016.10:67855887::GG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss80338546, ss82308770	NT_010498.15:21504000::GG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4302984022	NC_000016.10:67855887::GGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss4302984023	NC_000016.10:67855887::GGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
5435044973	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGGGG	NC_000016.10:67855887:GGGGGGGGGGG:… NC_000016.10:67855887:GGGGGGGGGGG:GGGGGGGGGGGGGGGG	(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 rs796843812

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
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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

rs796843812