Name: rs11429963
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.

rs11429963

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:114786912-114786932 (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(A)₁₂ / del(A)₁₁ / del(A)₁₀ / d…
del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₇ / del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₉ / dup(A)₁₂ / dup(A)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₀=0.000015 (4/264690, TOPMED)
del(A)₁₂=0.0000 (0/3354, ALFA)
del(A)₁₁=0.0000 (0/3354, ALFA) (+ 11 more)
del(A)₁₀=0.0000 (0/3354, ALFA)
del(A)₇=0.0000 (0/3354, ALFA)
del(A)₆=0.0000 (0/3354, ALFA)
del(A)₄=0.0000 (0/3354, ALFA)
delAAA=0.0000 (0/3354, ALFA)
delAA=0.0000 (0/3354, ALFA)
delA=0.0000 (0/3354, ALFA)
dupA=0.0000 (0/3354, ALFA)
dupAA=0.0000 (0/3354, ALFA)
dupAAA=0.0000 (0/3354, ALFA)
dup(A)₄=0.0000 (0/3354, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TNFSF15 : 3 Prime UTR 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	3354	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2514	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	518	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	26	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	492	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	28	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	24	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	46	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	128	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	12	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	108	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=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
TopMed	Global	Study-wide	264690	(A)₂₁=0.999985	del(A)₁₀=0.000015
Allele Frequency Aggregator	Total	Global	3354	(A)₂₁=1.0000	del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	2514	(A)₂₁=1.0000	del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	518	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	128	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	108	(A)₂₁=1.000	del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	28	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	12	(A)₂₁=1.00	del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)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 9	NC_000009.12:g.114786921_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786922_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786923_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786926_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786927_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786929_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786930_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786931_114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786932del
GRCh38.p14 chr 9	NC_000009.12:g.114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786931_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786930_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786929_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786928_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786927_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786926_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786925_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786924_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786921_114786932dup
GRCh38.p14 chr 9	NC_000009.12:g.114786920_114786932dup
GRCh37.p13 chr 9	NC_000009.11:g.117549201_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549202_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549203_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549206_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549207_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549209_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549210_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549211_117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549212del
GRCh37.p13 chr 9	NC_000009.11:g.117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549211_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549210_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549209_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549208_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549207_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549206_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549205_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549204_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549201_117549212dup
GRCh37.p13 chr 9	NC_000009.11:g.117549200_117549212dup
TNFSF15 RefSeqGene	NG_011488.2:g.24206_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24207_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24208_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24211_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24212_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24214_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24215_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24216_24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24217del
TNFSF15 RefSeqGene	NG_011488.2:g.24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24216_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24215_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24214_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24213_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24212_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24211_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24210_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24209_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24206_24217dup
TNFSF15 RefSeqGene	NG_011488.2:g.24205_24217dup

Gene: TNFSF15, TNF superfamily member 15 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TNFSF15 transcript variant 2	NM_001204344.1:c.3520_3… NM_001204344.1:c.3520_3540=	N/A	3 Prime UTR Variant
TNFSF15 transcript variant 1	NM_005118.4:c.3520_3540=	N/A	3 Prime UTR 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)₂₁=	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₇	del(A)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₉	dup(A)₁₂	dup(A)₁₃
GRCh38.p14 chr 9	NC_000009.12:g.114786912_114786932=	NC_000009.12:g.114786921_114786932del	NC_000009.12:g.114786922_114786932del	NC_000009.12:g.114786923_114786932del	NC_000009.12:g.114786926_114786932del	NC_000009.12:g.114786927_114786932del	NC_000009.12:g.114786929_114786932del	NC_000009.12:g.114786930_114786932del	NC_000009.12:g.114786931_114786932del	NC_000009.12:g.114786932del	NC_000009.12:g.114786932dup	NC_000009.12:g.114786931_114786932dup	NC_000009.12:g.114786930_114786932dup	NC_000009.12:g.114786929_114786932dup	NC_000009.12:g.114786928_114786932dup	NC_000009.12:g.114786927_114786932dup	NC_000009.12:g.114786926_114786932dup	NC_000009.12:g.114786925_114786932dup	NC_000009.12:g.114786924_114786932dup	NC_000009.12:g.114786921_114786932dup	NC_000009.12:g.114786920_114786932dup
GRCh37.p13 chr 9	NC_000009.11:g.117549192_117549212=	NC_000009.11:g.117549201_117549212del	NC_000009.11:g.117549202_117549212del	NC_000009.11:g.117549203_117549212del	NC_000009.11:g.117549206_117549212del	NC_000009.11:g.117549207_117549212del	NC_000009.11:g.117549209_117549212del	NC_000009.11:g.117549210_117549212del	NC_000009.11:g.117549211_117549212del	NC_000009.11:g.117549212del	NC_000009.11:g.117549212dup	NC_000009.11:g.117549211_117549212dup	NC_000009.11:g.117549210_117549212dup	NC_000009.11:g.117549209_117549212dup	NC_000009.11:g.117549208_117549212dup	NC_000009.11:g.117549207_117549212dup	NC_000009.11:g.117549206_117549212dup	NC_000009.11:g.117549205_117549212dup	NC_000009.11:g.117549204_117549212dup	NC_000009.11:g.117549201_117549212dup	NC_000009.11:g.117549200_117549212dup
TNFSF15 RefSeqGene	NG_011488.2:g.24197_24217=	NG_011488.2:g.24206_24217del	NG_011488.2:g.24207_24217del	NG_011488.2:g.24208_24217del	NG_011488.2:g.24211_24217del	NG_011488.2:g.24212_24217del	NG_011488.2:g.24214_24217del	NG_011488.2:g.24215_24217del	NG_011488.2:g.24216_24217del	NG_011488.2:g.24217del	NG_011488.2:g.24217dup	NG_011488.2:g.24216_24217dup	NG_011488.2:g.24215_24217dup	NG_011488.2:g.24214_24217dup	NG_011488.2:g.24213_24217dup	NG_011488.2:g.24212_24217dup	NG_011488.2:g.24211_24217dup	NG_011488.2:g.24210_24217dup	NG_011488.2:g.24209_24217dup	NG_011488.2:g.24206_24217dup	NG_011488.2:g.24205_24217dup
TNFSF15 transcript variant 1	NM_005118.4:c.3520_3540=	NM_005118.4:c.3529_3540del	NM_005118.4:c.3530_3540del	NM_005118.4:c.3531_3540del	NM_005118.4:c.3534_3540del	NM_005118.4:c.3535_3540del	NM_005118.4:c.3537_3540del	NM_005118.4:c.3538_3540del	NM_005118.4:c.3539_3540del	NM_005118.4:c.*3540del	NM_005118.4:c.*3540dup	NM_005118.4:c.3539_3540dup	NM_005118.4:c.3538_3540dup	NM_005118.4:c.3537_3540dup	NM_005118.4:c.3536_3540dup	NM_005118.4:c.3535_3540dup	NM_005118.4:c.3534_3540dup	NM_005118.4:c.3533_3540dup	NM_005118.4:c.3532_3540dup	NM_005118.4:c.3529_3540dup	NM_005118.4:c.3528_3540dup
TNFSF15 transcript variant 1	NM_005118.3:c.3520_3540=	NM_005118.3:c.3529_3540del	NM_005118.3:c.3530_3540del	NM_005118.3:c.3531_3540del	NM_005118.3:c.3534_3540del	NM_005118.3:c.3535_3540del	NM_005118.3:c.3537_3540del	NM_005118.3:c.3538_3540del	NM_005118.3:c.3539_3540del	NM_005118.3:c.*3540del	NM_005118.3:c.*3540dup	NM_005118.3:c.3539_3540dup	NM_005118.3:c.3538_3540dup	NM_005118.3:c.3537_3540dup	NM_005118.3:c.3536_3540dup	NM_005118.3:c.3535_3540dup	NM_005118.3:c.3534_3540dup	NM_005118.3:c.3533_3540dup	NM_005118.3:c.3532_3540dup	NM_005118.3:c.3529_3540dup	NM_005118.3:c.3528_3540dup
TNFSF15 transcript variant 2	NM_001204344.1:c.3520_3540=	NM_001204344.1:c.3529_3540del	NM_001204344.1:c.3530_3540del	NM_001204344.1:c.3531_3540del	NM_001204344.1:c.3534_3540del	NM_001204344.1:c.3535_3540del	NM_001204344.1:c.3537_3540del	NM_001204344.1:c.3538_3540del	NM_001204344.1:c.3539_3540del	NM_001204344.1:c.*3540del	NM_001204344.1:c.*3540dup	NM_001204344.1:c.3539_3540dup	NM_001204344.1:c.3538_3540dup	NM_001204344.1:c.3537_3540dup	NM_001204344.1:c.3536_3540dup	NM_001204344.1:c.3535_3540dup	NM_001204344.1:c.3534_3540dup	NM_001204344.1:c.3533_3540dup	NM_001204344.1:c.3532_3540dup	NM_001204344.1:c.3529_3540dup	NM_001204344.1:c.3528_3540dup

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#.

54 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43415231	Mar 13, 2006 (126)
2	CGM_KYOTO	ss76868220	Dec 04, 2013 (138)
3	HGSV	ss80126341	Dec 15, 2007 (130)
4	CNG	ss98338483	Feb 06, 2009 (130)
5	PJP	ss295436268	May 09, 2011 (138)
6	EVA_UK10K_ALSPAC	ss1706535785	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1706535787	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1706535883	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1706535884	Apr 01, 2015 (144)
10	SWEGEN	ss3005492995	Jan 10, 2018 (151)
11	EVA_DECODE	ss3724631454	Jul 13, 2019 (153)
12	EVA_DECODE	ss3724631455	Jul 13, 2019 (153)
13	EVA_DECODE	ss3724631456	Jul 13, 2019 (153)
14	EVA_DECODE	ss3724631457	Jul 13, 2019 (153)
15	EVA	ss3831830387	Apr 26, 2020 (154)
16	GNOMAD	ss4208353389	Apr 26, 2021 (155)
17	GNOMAD	ss4208353390	Apr 26, 2021 (155)
18	GNOMAD	ss4208353391	Apr 26, 2021 (155)
19	GNOMAD	ss4208353392	Apr 26, 2021 (155)
20	GNOMAD	ss4208353393	Apr 26, 2021 (155)
21	GNOMAD	ss4208353394	Apr 26, 2021 (155)
22	GNOMAD	ss4208353395	Apr 26, 2021 (155)
23	GNOMAD	ss4208353396	Apr 26, 2021 (155)
24	GNOMAD	ss4208353397	Apr 26, 2021 (155)
25	GNOMAD	ss4208353398	Apr 26, 2021 (155)
26	GNOMAD	ss4208353399	Apr 26, 2021 (155)
27	GNOMAD	ss4208353400	Apr 26, 2021 (155)
28	GNOMAD	ss4208353401	Apr 26, 2021 (155)
29	GNOMAD	ss4208353402	Apr 26, 2021 (155)
30	GNOMAD	ss4208353403	Apr 26, 2021 (155)
31	GNOMAD	ss4208353404	Apr 26, 2021 (155)
32	GNOMAD	ss4208353405	Apr 26, 2021 (155)
33	GNOMAD	ss4208353406	Apr 26, 2021 (155)
34	TOPMED	ss4833462409	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5195016739	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5195016740	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5195016741	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5195016742	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5195016743	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5195016744	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5281967812	Oct 16, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5281967813	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5281967814	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5281967815	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5477855799	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5477855800	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5477855801	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5477855802	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5477855803	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5739463051	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5739463052	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5739463053	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5739463054	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5739463056	Oct 16, 2022 (156)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26404838 (NC_000009.11:117549191::AA 876/3854) Row 26404839 (NC_000009.11:117549191::A 1743/3854)	-	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 26404838 (NC_000009.11:117549191::AA 876/3854) Row 26404839 (NC_000009.11:117549191::A 1743/3854)	-	Oct 12, 2018 (152)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 335856224 (NC_000009.12:114786911::A 36049/73658) Row 335856225 (NC_000009.12:114786911::AA 495/73568) Row 335856226 (NC_000009.12:114786911::AAA 46/73752)...	-	Apr 26, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 52986046 (NC_000009.11:117549191::A 6147/16132) Row 52986047 (NC_000009.11:117549191:A: 1098/16132) Row 52986048 (NC_000009.11:117549191:AA: 184/16132)...	-	Apr 26, 2021 (155)
81	14KJPN Submission ignored due to conflicting rows: Row 73300155 (NC_000009.12:114786911::A 11288/27834) Row 73300156 (NC_000009.12:114786911::AAAAAAA 55/27834) Row 73300157 (NC_000009.12:114786911:AA: 344/27834)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 73300155 (NC_000009.12:114786911::A 11288/27834) Row 73300156 (NC_000009.12:114786911::AAAAAAA 55/27834) Row 73300157 (NC_000009.12:114786911:AA: 344/27834)...	-	Oct 16, 2022 (156)
83	14KJPN Submission ignored due to conflicting rows: Row 73300155 (NC_000009.12:114786911::A 11288/27834) Row 73300156 (NC_000009.12:114786911::AAAAAAA 55/27834) Row 73300157 (NC_000009.12:114786911:AA: 344/27834)...	-	Oct 16, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 73300155 (NC_000009.12:114786911::A 11288/27834) Row 73300156 (NC_000009.12:114786911::AAAAAAA 55/27834) Row 73300157 (NC_000009.12:114786911:AA: 344/27834)...	-	Oct 16, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 73300155 (NC_000009.12:114786911::A 11288/27834) Row 73300156 (NC_000009.12:114786911::AAAAAAA 55/27834) Row 73300157 (NC_000009.12:114786911:AA: 344/27834)...	-	Oct 16, 2022 (156)
86	TopMed	NC_000009.12 - 114786912	Apr 26, 2021 (155)
87	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26404838 (NC_000009.11:117549191::AA 810/3708) Row 26404839 (NC_000009.11:117549191::A 1694/3708)	-	Oct 12, 2018 (152)
88	UK 10K study - Twins Submission ignored due to conflicting rows: Row 26404838 (NC_000009.11:117549191::AA 810/3708) Row 26404839 (NC_000009.11:117549191::A 1694/3708)	-	Oct 12, 2018 (152)
89	ALFA	NC_000009.12 - 114786912	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)
rs11447153	May 11, 2012 (137)
rs34459117	May 11, 2012 (137)
rs58882962	May 23, 2008 (130)
rs71743774	May 11, 2012 (137)
rs71748172	May 11, 2012 (137)
rs72505936	May 11, 2012 (137)
rs141245595	Apr 25, 2013 (138)
rs55853037	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4208353406	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
670839970, ss4208353405, ss4833462409	NC_000009.12:114786911:AAAAAAAAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4208353404	NC_000009.12:114786911:AAAAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4208353403	NC_000009.12:114786911:AAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4208353402	NC_000009.12:114786911:AAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3005492995, ss5195016741	NC_000009.11:117549191:AA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3724631457, ss4208353401, ss5281967813, ss5477855803, ss5739463053	NC_000009.12:114786911:AA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5195016740	NC_000009.11:117549191:A:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4208353400, ss5281967814, ss5477855800, ss5739463054	NC_000009.12:114786911:A:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3724631456	NC_000009.12:114786912:A:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss43415231, ss98338483	NT_008470.19:46713723:A:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss76868220	NT_008470.19:46713724:A:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss295436268	NC_000009.10:116589033::A	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1706535787, ss1706535884, ss3831830387, ss5195016739	NC_000009.11:117549191::A	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353389, ss5281967812, ss5477855799, ss5739463051	NC_000009.12:114786911::A	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724631455	NC_000009.12:114786913::A	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss80126341	NT_008470.19:46713744::A	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss1706535785, ss1706535883, ss5195016744	NC_000009.11:117549191::AA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353390, ss5281967815, ss5477855801, ss5739463056	NC_000009.12:114786911::AA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3724631454	NC_000009.12:114786913::AA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353391, ss5477855802	NC_000009.12:114786911::AAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353392	NC_000009.12:114786911::AAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
8310480562	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353393	NC_000009.12:114786911::AAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5195016743	NC_000009.11:117549191::AAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353394	NC_000009.12:114786911::AAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5195016742	NC_000009.11:117549191::AAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353395, ss5739463052	NC_000009.12:114786911::AAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353396	NC_000009.12:114786911::AAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353397	NC_000009.12:114786911::AAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353398	NC_000009.12:114786911::AAAAAAAAAA… NC_000009.12:114786911::AAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4208353399	NC_000009.12:114786911::AAAAAAAAAA… NC_000009.12:114786911::AAAAAAAAAAAAA	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3598973402	NC_000009.12:114786911:AAAAAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA
ss3598973404	NC_000009.12:114786911:AAAAAAAAAAA:	NC_000009.12:114786911:AAAAAAAAAAA… NC_000009.12:114786911:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs11429963

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

rs11429963