Name: rs966796673
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.

rs966796673

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:70226192-70226204 (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: delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.00005 (1/18506, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SRSF11 : 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	18506	AAAAAAAAAAAAA=0.99995	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00005	0.999892	0.000108	0
European	Sub	14144	AAAAAAAAAAAAA=0.99993	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00007	0.999859	0.000141	0
African	Sub	2894	AAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
African Others	Sub	114	AAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
African American	Sub	2780	AAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
Asian	Sub	112	AAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
East Asian	Sub	86	AAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other Asian	Sub	26	AAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Latin American 1	Sub	146	AAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
Latin American 2	Sub	608	AAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
South Asian	Sub	98	AAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other	Sub	504	AAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	18506	(A)₁₃=0.99995	delA=0.00000, dupA=0.00005
Allele Frequency Aggregator	European	Sub	14144	(A)₁₃=0.99993	delA=0.00000, dupA=0.00007
Allele Frequency Aggregator	African	Sub	2894	(A)₁₃=1.0000	delA=0.0000, dupA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	608	(A)₁₃=1.000	delA=0.000, dupA=0.000
Allele Frequency Aggregator	Other	Sub	504	(A)₁₃=1.000	delA=0.000, dupA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(A)₁₃=1.000	delA=0.000, dupA=0.000
Allele Frequency Aggregator	Asian	Sub	112	(A)₁₃=1.000	delA=0.000, dupA=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(A)₁₃=1.00	delA=0.00, dupA=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 1	NC_000001.11:g.70226204del
GRCh38.p14 chr 1	NC_000001.11:g.70226204dup
GRCh38.p14 chr 1	NC_000001.11:g.70226203_70226204dup
GRCh37.p13 chr 1	NC_000001.10:g.70691887del
GRCh37.p13 chr 1	NC_000001.10:g.70691887dup
GRCh37.p13 chr 1	NC_000001.10:g.70691886_70691887dup

Gene: SRSF11, serine and arginine rich splicing factor 11 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SRSF11 transcript variant 2	NM_001190987.3:c.204-2218… NM_001190987.3:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 3	NM_001350605.2:c.204-2218… NM_001350605.2:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 4	NM_001350606.2:c.204-2218… NM_001350606.2:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 5	NM_001350607.2:c.204-2218… NM_001350607.2:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 6	NM_001350608.2:c.204-2218… NM_001350608.2:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 7	NM_001350609.2:c.204-2218… NM_001350609.2:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 8	NM_001350610.2:c.-484-221… NM_001350610.2:c.-484-2218del	N/A	Intron Variant
SRSF11 transcript variant 9	NM_001350611.2:c.-484-221… NM_001350611.2:c.-484-2218del	N/A	Intron Variant
SRSF11 transcript variant 10	NM_001350612.2:c.-593-221… NM_001350612.2:c.-593-2218del	N/A	Intron Variant
SRSF11 transcript variant 11	NM_001350613.2:c.-484-221… NM_001350613.2:c.-484-2218del	N/A	Intron Variant
SRSF11 transcript variant 12	NM_001350614.2:c.-593-221… NM_001350614.2:c.-593-2218del	N/A	Intron Variant
SRSF11 transcript variant 13	NM_001350615.2:c.-367-221… NM_001350615.2:c.-367-2218del	N/A	Intron Variant
SRSF11 transcript variant 14	NM_001350616.2:c.-484-221… NM_001350616.2:c.-484-2218del	N/A	Intron Variant
SRSF11 transcript variant 16	NM_001394402.1:c.237-2218… NM_001394402.1:c.237-2218del	N/A	Intron Variant
SRSF11 transcript variant 17	NM_001394403.1:c.237-2218… NM_001394403.1:c.237-2218del	N/A	Intron Variant
SRSF11 transcript variant 18	NM_001394404.1:c.204-2218… NM_001394404.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 19	NM_001394405.1:c.204-2218… NM_001394405.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 20	NM_001394406.1:c.204-2218… NM_001394406.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 21	NM_001394407.1:c.204-2218… NM_001394407.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 22	NM_001394408.1:c.204-2218… NM_001394408.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 1	NM_004768.5:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant 15	NR_146810.2:n.	N/A	Intron Variant
SRSF11 transcript variant X1	XM_047434514.1:c.204-2218… XM_047434514.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X2	XM_047434516.1:c.204-2218… XM_047434516.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X3	XM_047434517.1:c.204-2218… XM_047434517.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X4	XM_047434518.1:c.204-2218… XM_047434518.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X5	XM_047434522.1:c.204-2218… XM_047434522.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X6	XM_047434523.1:c.204-2218… XM_047434523.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X7	XM_047434524.1:c.204-2218… XM_047434524.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X10	XM_047434541.1:c.204-2218… XM_047434541.1:c.204-2218del	N/A	Intron Variant
SRSF11 transcript variant X8	XM_024450906.2:c.	N/A	Genic Upstream Transcript Variant
SRSF11 transcript variant X9	XM_047434536.1:c.	N/A	Genic 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	(A)₁₃=	delA	dupA	dupAA
GRCh38.p14 chr 1	NC_000001.11:g.70226192_70226204=	NC_000001.11:g.70226204del	NC_000001.11:g.70226204dup	NC_000001.11:g.70226203_70226204dup
GRCh37.p13 chr 1	NC_000001.10:g.70691875_70691887=	NC_000001.10:g.70691887del	NC_000001.10:g.70691887dup	NC_000001.10:g.70691886_70691887dup
SRSF11 transcript variant 2	NM_001190987.1:c.204-2230=	NM_001190987.1:c.204-2218del	NM_001190987.1:c.204-2218dup	NM_001190987.1:c.204-2219_204-2218dup
SRSF11 transcript variant 2	NM_001190987.3:c.204-2230=	NM_001190987.3:c.204-2218del	NM_001190987.3:c.204-2218dup	NM_001190987.3:c.204-2219_204-2218dup
SRSF11 transcript variant 3	NM_001350605.2:c.204-2230=	NM_001350605.2:c.204-2218del	NM_001350605.2:c.204-2218dup	NM_001350605.2:c.204-2219_204-2218dup
SRSF11 transcript variant 4	NM_001350606.2:c.204-2230=	NM_001350606.2:c.204-2218del	NM_001350606.2:c.204-2218dup	NM_001350606.2:c.204-2219_204-2218dup
SRSF11 transcript variant 5	NM_001350607.2:c.204-2230=	NM_001350607.2:c.204-2218del	NM_001350607.2:c.204-2218dup	NM_001350607.2:c.204-2219_204-2218dup
SRSF11 transcript variant 6	NM_001350608.2:c.204-2230=	NM_001350608.2:c.204-2218del	NM_001350608.2:c.204-2218dup	NM_001350608.2:c.204-2219_204-2218dup
SRSF11 transcript variant 7	NM_001350609.2:c.204-2230=	NM_001350609.2:c.204-2218del	NM_001350609.2:c.204-2218dup	NM_001350609.2:c.204-2219_204-2218dup
SRSF11 transcript variant 8	NM_001350610.2:c.-484-2230=	NM_001350610.2:c.-484-2218del	NM_001350610.2:c.-484-2218dup	NM_001350610.2:c.-484-2219_-484-2218dup
SRSF11 transcript variant 9	NM_001350611.2:c.-484-2230=	NM_001350611.2:c.-484-2218del	NM_001350611.2:c.-484-2218dup	NM_001350611.2:c.-484-2219_-484-2218dup
SRSF11 transcript variant 10	NM_001350612.2:c.-593-2230=	NM_001350612.2:c.-593-2218del	NM_001350612.2:c.-593-2218dup	NM_001350612.2:c.-593-2219_-593-2218dup
SRSF11 transcript variant 11	NM_001350613.2:c.-484-2230=	NM_001350613.2:c.-484-2218del	NM_001350613.2:c.-484-2218dup	NM_001350613.2:c.-484-2219_-484-2218dup
SRSF11 transcript variant 12	NM_001350614.2:c.-593-2230=	NM_001350614.2:c.-593-2218del	NM_001350614.2:c.-593-2218dup	NM_001350614.2:c.-593-2219_-593-2218dup
SRSF11 transcript variant 13	NM_001350615.2:c.-367-2230=	NM_001350615.2:c.-367-2218del	NM_001350615.2:c.-367-2218dup	NM_001350615.2:c.-367-2219_-367-2218dup
SRSF11 transcript variant 14	NM_001350616.2:c.-484-2230=	NM_001350616.2:c.-484-2218del	NM_001350616.2:c.-484-2218dup	NM_001350616.2:c.-484-2219_-484-2218dup
SRSF11 transcript variant 16	NM_001394402.1:c.237-2230=	NM_001394402.1:c.237-2218del	NM_001394402.1:c.237-2218dup	NM_001394402.1:c.237-2219_237-2218dup
SRSF11 transcript variant 17	NM_001394403.1:c.237-2230=	NM_001394403.1:c.237-2218del	NM_001394403.1:c.237-2218dup	NM_001394403.1:c.237-2219_237-2218dup
SRSF11 transcript variant 18	NM_001394404.1:c.204-2230=	NM_001394404.1:c.204-2218del	NM_001394404.1:c.204-2218dup	NM_001394404.1:c.204-2219_204-2218dup
SRSF11 transcript variant 19	NM_001394405.1:c.204-2230=	NM_001394405.1:c.204-2218del	NM_001394405.1:c.204-2218dup	NM_001394405.1:c.204-2219_204-2218dup
SRSF11 transcript variant 20	NM_001394406.1:c.204-2230=	NM_001394406.1:c.204-2218del	NM_001394406.1:c.204-2218dup	NM_001394406.1:c.204-2219_204-2218dup
SRSF11 transcript variant 21	NM_001394407.1:c.204-2230=	NM_001394407.1:c.204-2218del	NM_001394407.1:c.204-2218dup	NM_001394407.1:c.204-2219_204-2218dup
SRSF11 transcript variant 22	NM_001394408.1:c.204-2230=	NM_001394408.1:c.204-2218del	NM_001394408.1:c.204-2218dup	NM_001394408.1:c.204-2219_204-2218dup
SRSF11 transcript variant 1	NM_004768.3:c.204-2230=	NM_004768.3:c.204-2218del	NM_004768.3:c.204-2218dup	NM_004768.3:c.204-2219_204-2218dup
SRSF11 transcript variant 1	NM_004768.5:c.204-2230=	NM_004768.5:c.204-2218del	NM_004768.5:c.204-2218dup	NM_004768.5:c.204-2219_204-2218dup
SRSF11 transcript variant X1	XM_005271338.1:c.204-2230=	XM_005271338.1:c.204-2218del	XM_005271338.1:c.204-2218dup	XM_005271338.1:c.204-2219_204-2218dup
SRSF11 transcript variant X2	XM_005271339.1:c.204-2230=	XM_005271339.1:c.204-2218del	XM_005271339.1:c.204-2218dup	XM_005271339.1:c.204-2219_204-2218dup
SRSF11 transcript variant X3	XM_005271340.1:c.204-2230=	XM_005271340.1:c.204-2218del	XM_005271340.1:c.204-2218dup	XM_005271340.1:c.204-2219_204-2218dup
SRSF11 transcript variant X4	XM_005271341.1:c.204-2230=	XM_005271341.1:c.204-2218del	XM_005271341.1:c.204-2218dup	XM_005271341.1:c.204-2219_204-2218dup
SRSF11 transcript variant X5	XM_005271342.1:c.-1150-2230=	XM_005271342.1:c.-1150-2218del	XM_005271342.1:c.-1150-2218dup	XM_005271342.1:c.-1150-2219_-1150-2218dup
SRSF11 transcript variant X6	XM_005271343.1:c.-495-2230=	XM_005271343.1:c.-495-2218del	XM_005271343.1:c.-495-2218dup	XM_005271343.1:c.-495-2219_-495-2218dup
SRSF11 transcript variant X7	XM_005271344.1:c.-1150-2230=	XM_005271344.1:c.-1150-2218del	XM_005271344.1:c.-1150-2218dup	XM_005271344.1:c.-1150-2219_-1150-2218dup
SRSF11 transcript variant X8	XM_005271345.1:c.-1248-2230=	XM_005271345.1:c.-1248-2218del	XM_005271345.1:c.-1248-2218dup	XM_005271345.1:c.-1248-2219_-1248-2218dup
SRSF11 transcript variant X9	XM_005271346.1:c.-3787-2230=	XM_005271346.1:c.-3787-2218del	XM_005271346.1:c.-3787-2218dup	XM_005271346.1:c.-3787-2219_-3787-2218dup
SRSF11 transcript variant X1	XM_047434514.1:c.204-2230=	XM_047434514.1:c.204-2218del	XM_047434514.1:c.204-2218dup	XM_047434514.1:c.204-2219_204-2218dup
SRSF11 transcript variant X2	XM_047434516.1:c.204-2230=	XM_047434516.1:c.204-2218del	XM_047434516.1:c.204-2218dup	XM_047434516.1:c.204-2219_204-2218dup
SRSF11 transcript variant X3	XM_047434517.1:c.204-2230=	XM_047434517.1:c.204-2218del	XM_047434517.1:c.204-2218dup	XM_047434517.1:c.204-2219_204-2218dup
SRSF11 transcript variant X4	XM_047434518.1:c.204-2230=	XM_047434518.1:c.204-2218del	XM_047434518.1:c.204-2218dup	XM_047434518.1:c.204-2219_204-2218dup
SRSF11 transcript variant X5	XM_047434522.1:c.204-2230=	XM_047434522.1:c.204-2218del	XM_047434522.1:c.204-2218dup	XM_047434522.1:c.204-2219_204-2218dup
SRSF11 transcript variant X6	XM_047434523.1:c.204-2230=	XM_047434523.1:c.204-2218del	XM_047434523.1:c.204-2218dup	XM_047434523.1:c.204-2219_204-2218dup
SRSF11 transcript variant X7	XM_047434524.1:c.204-2230=	XM_047434524.1:c.204-2218del	XM_047434524.1:c.204-2218dup	XM_047434524.1:c.204-2219_204-2218dup
SRSF11 transcript variant X10	XM_047434541.1:c.204-2230=	XM_047434541.1:c.204-2218del	XM_047434541.1:c.204-2218dup	XM_047434541.1:c.204-2219_204-2218dup

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#.

5 SubSNP, 4 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PACBIO	ss3783439235	Jul 12, 2019 (153)
2	GNOMAD	ss3995485470	Apr 25, 2021 (155)
3	GNOMAD	ss3995485471	Apr 25, 2021 (155)
4	HUGCELL_USP	ss5443660940	Oct 12, 2022 (156)
5	YY_MCH	ss5800687492	Oct 12, 2022 (156)
6	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14438662 (NC_000001.11:70226191::A 90/124326) Row 14438663 (NC_000001.11:70226191::AA 1/124416) Row 14438664 (NC_000001.11:70226191:A: 102/124238)	-	Apr 25, 2021 (155)
7	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14438662 (NC_000001.11:70226191::A 90/124326) Row 14438663 (NC_000001.11:70226191::AA 1/124416) Row 14438664 (NC_000001.11:70226191:A: 102/124238)	-	Apr 25, 2021 (155)
8	gnomAD - Genomes Submission ignored due to conflicting rows: Row 14438662 (NC_000001.11:70226191::A 90/124326) Row 14438663 (NC_000001.11:70226191::AA 1/124416) Row 14438664 (NC_000001.11:70226191:A: 102/124238)	-	Apr 25, 2021 (155)
9	ALFA	NC_000001.11 - 70226192	Apr 25, 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
ss3783439235	NC_000001.10:70691874:A:	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
	NC_000001.11:70226191:A:	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
277251869	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3995485470, ss5443660940, ss5800687492	NC_000001.11:70226191::A	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
277251869	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3995485471	NC_000001.11:70226191::AA	NC_000001.11:70226191:AAAAAAAAAAAA… NC_000001.11:70226191:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(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 rs966796673

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

rs966796673