Name: rs71025383
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.

rs71025383

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:92025811-92025832 (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)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₇ / del(A)₅ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₈ / dup(A)₉ / dup(A)₁₀ / dup(A)₁₂ / dup(A)₁₄ / dup(A)₁₇ / ins(A)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.0000 (0/1816, ALFA)
del(A)₁₃=0.0000 (0/1816, ALFA)
del(A)₁₂=0.0000 (0/1816, ALFA) (+ 13 more)
del(A)₁₁=0.0000 (0/1816, ALFA)
del(A)₁₀=0.0000 (0/1816, ALFA)
del(A)₈=0.0000 (0/1816, ALFA)
del(A)₇=0.0000 (0/1816, ALFA)
del(A)₅=0.0000 (0/1816, ALFA)
delAA=0.0000 (0/1816, ALFA)
delA=0.0000 (0/1816, ALFA)
dupA=0.0000 (0/1816, ALFA)
dupAA=0.0000 (0/1816, ALFA)
dupAAA=0.0000 (0/1816, ALFA)
dup(A)₄=0.0000 (0/1816, ALFA)
dup(A)₅=0.0000 (0/1816, ALFA)
dup(A)₆=0.0000 (0/1816, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BTAF1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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	1816	(A)₂₂=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	European	Sub	1436	(A)₂₂=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₅=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000, dup(A)₆=0.0000
Allele Frequency Aggregator	African	Sub	222	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₅=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000, dup(A)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	56	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Other	Sub	56	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	28	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	Asian	Sub	14	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₅=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00, dup(A)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(A)₂₂=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₅=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₄=0.0, dup(A)₅=0.0, dup(A)₆=0.0

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 10	NC_000010.11:g.92025819_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025820_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025821_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025822_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025823_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025825_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025826_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025828_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025830_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025831_92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025832del
GRCh38.p14 chr 10	NC_000010.11:g.92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025831_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025830_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025829_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025828_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025827_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025825_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025824_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025823_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025821_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025819_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025816_92025832dup
GRCh38.p14 chr 10	NC_000010.11:g.92025832_92025833insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.93785576_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785577_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785578_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785579_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785580_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785582_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785583_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785585_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785587_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785588_93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785589del
GRCh37.p13 chr 10	NC_000010.10:g.93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785588_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785587_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785586_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785585_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785584_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785582_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785581_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785580_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785578_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785576_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785573_93785589dup
GRCh37.p13 chr 10	NC_000010.10:g.93785589_93785590insAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: BTAF1, B-TFIID TATA-box binding protein associated factor 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BTAF1 transcript variant 1	NM_003972.3:c.5076-773_50… NM_003972.3:c.5076-773_5076-760del	N/A	Intron Variant
BTAF1 transcript variant 2	NR_165090.1:n.	N/A	Intron Variant
BTAF1 transcript variant 3	NR_165091.1:n.	N/A	Intron Variant
BTAF1 transcript variant 4	NR_165092.1:n.	N/A	Intron Variant
BTAF1 transcript variant 5	NR_165093.1:n.	N/A	Intron Variant
BTAF1 transcript variant 6	NR_165094.1:n.	N/A	Intron Variant
BTAF1 transcript variant 7	NR_165095.1:n.	N/A	Intron Variant
BTAF1 transcript variant 8	NR_165096.1:n.	N/A	Intron Variant
BTAF1 transcript variant 9	NR_165097.1:n.	N/A	Intron Variant
BTAF1 transcript variant 10	NR_165098.1:n.	N/A	Intron Variant
BTAF1 transcript variant 11	NR_165099.1:n.	N/A	Intron Variant
BTAF1 transcript variant 13	NR_165101.1:n.	N/A	Intron Variant
BTAF1 transcript variant 14	NR_165102.1:n.	N/A	Intron Variant
BTAF1 transcript variant 15	NR_165103.1:n.	N/A	Intron Variant
BTAF1 transcript variant 16	NR_165104.1:n.	N/A	Intron Variant
BTAF1 transcript variant X1	XM_011540326.3:c.4965-773… XM_011540326.3:c.4965-773_4965-760del	N/A	Intron Variant
BTAF1 transcript variant X3	XM_011540327.3:c.4704-773… XM_011540327.3:c.4704-773_4704-760del	N/A	Intron Variant
BTAF1 transcript variant X4	XM_011540328.3:c.4608-773… XM_011540328.3:c.4608-773_4608-760del	N/A	Intron Variant
BTAF1 transcript variant X2	XM_017016877.2:c.4929-773… XM_017016877.2:c.4929-773_4929-760del	N/A	Intron Variant
BTAF1 transcript variant X5	XM_047425989.1:c.4086-773… XM_047425989.1:c.4086-773_4086-760del	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	(A)₂₂=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₇	del(A)₅	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₈	dup(A)₉	dup(A)₁₀	dup(A)₁₂	dup(A)₁₄	dup(A)₁₇	ins(A)₂₆
GRCh38.p14 chr 10	NC_000010.11:g.92025811_92025832=	NC_000010.11:g.92025819_92025832del	NC_000010.11:g.92025820_92025832del	NC_000010.11:g.92025821_92025832del	NC_000010.11:g.92025822_92025832del	NC_000010.11:g.92025823_92025832del	NC_000010.11:g.92025825_92025832del	NC_000010.11:g.92025826_92025832del	NC_000010.11:g.92025828_92025832del	NC_000010.11:g.92025830_92025832del	NC_000010.11:g.92025831_92025832del	NC_000010.11:g.92025832del	NC_000010.11:g.92025832dup	NC_000010.11:g.92025831_92025832dup	NC_000010.11:g.92025830_92025832dup	NC_000010.11:g.92025829_92025832dup	NC_000010.11:g.92025828_92025832dup	NC_000010.11:g.92025827_92025832dup	NC_000010.11:g.92025825_92025832dup	NC_000010.11:g.92025824_92025832dup	NC_000010.11:g.92025823_92025832dup	NC_000010.11:g.92025821_92025832dup	NC_000010.11:g.92025819_92025832dup	NC_000010.11:g.92025816_92025832dup	NC_000010.11:g.92025832_92025833insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 10	NC_000010.10:g.93785568_93785589=	NC_000010.10:g.93785576_93785589del	NC_000010.10:g.93785577_93785589del	NC_000010.10:g.93785578_93785589del	NC_000010.10:g.93785579_93785589del	NC_000010.10:g.93785580_93785589del	NC_000010.10:g.93785582_93785589del	NC_000010.10:g.93785583_93785589del	NC_000010.10:g.93785585_93785589del	NC_000010.10:g.93785587_93785589del	NC_000010.10:g.93785588_93785589del	NC_000010.10:g.93785589del	NC_000010.10:g.93785589dup	NC_000010.10:g.93785588_93785589dup	NC_000010.10:g.93785587_93785589dup	NC_000010.10:g.93785586_93785589dup	NC_000010.10:g.93785585_93785589dup	NC_000010.10:g.93785584_93785589dup	NC_000010.10:g.93785582_93785589dup	NC_000010.10:g.93785581_93785589dup	NC_000010.10:g.93785580_93785589dup	NC_000010.10:g.93785578_93785589dup	NC_000010.10:g.93785576_93785589dup	NC_000010.10:g.93785573_93785589dup	NC_000010.10:g.93785589_93785590insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript	NM_003972.2:c.5076-781=	NM_003972.2:c.5076-773_5076-760del	NM_003972.2:c.5076-772_5076-760del	NM_003972.2:c.5076-771_5076-760del	NM_003972.2:c.5076-770_5076-760del	NM_003972.2:c.5076-769_5076-760del	NM_003972.2:c.5076-767_5076-760del	NM_003972.2:c.5076-766_5076-760del	NM_003972.2:c.5076-764_5076-760del	NM_003972.2:c.5076-762_5076-760del	NM_003972.2:c.5076-761_5076-760del	NM_003972.2:c.5076-760del	NM_003972.2:c.5076-760dup	NM_003972.2:c.5076-761_5076-760dup	NM_003972.2:c.5076-762_5076-760dup	NM_003972.2:c.5076-763_5076-760dup	NM_003972.2:c.5076-764_5076-760dup	NM_003972.2:c.5076-765_5076-760dup	NM_003972.2:c.5076-767_5076-760dup	NM_003972.2:c.5076-768_5076-760dup	NM_003972.2:c.5076-769_5076-760dup	NM_003972.2:c.5076-771_5076-760dup	NM_003972.2:c.5076-773_5076-760dup	NM_003972.2:c.5076-776_5076-760dup	NM_003972.2:c.5076-760_5076-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant 1	NM_003972.3:c.5076-781=	NM_003972.3:c.5076-773_5076-760del	NM_003972.3:c.5076-772_5076-760del	NM_003972.3:c.5076-771_5076-760del	NM_003972.3:c.5076-770_5076-760del	NM_003972.3:c.5076-769_5076-760del	NM_003972.3:c.5076-767_5076-760del	NM_003972.3:c.5076-766_5076-760del	NM_003972.3:c.5076-764_5076-760del	NM_003972.3:c.5076-762_5076-760del	NM_003972.3:c.5076-761_5076-760del	NM_003972.3:c.5076-760del	NM_003972.3:c.5076-760dup	NM_003972.3:c.5076-761_5076-760dup	NM_003972.3:c.5076-762_5076-760dup	NM_003972.3:c.5076-763_5076-760dup	NM_003972.3:c.5076-764_5076-760dup	NM_003972.3:c.5076-765_5076-760dup	NM_003972.3:c.5076-767_5076-760dup	NM_003972.3:c.5076-768_5076-760dup	NM_003972.3:c.5076-769_5076-760dup	NM_003972.3:c.5076-771_5076-760dup	NM_003972.3:c.5076-773_5076-760dup	NM_003972.3:c.5076-776_5076-760dup	NM_003972.3:c.5076-760_5076-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X1	XM_005270265.1:c.4467-781=	XM_005270265.1:c.4467-773_4467-760del	XM_005270265.1:c.4467-772_4467-760del	XM_005270265.1:c.4467-771_4467-760del	XM_005270265.1:c.4467-770_4467-760del	XM_005270265.1:c.4467-769_4467-760del	XM_005270265.1:c.4467-767_4467-760del	XM_005270265.1:c.4467-766_4467-760del	XM_005270265.1:c.4467-764_4467-760del	XM_005270265.1:c.4467-762_4467-760del	XM_005270265.1:c.4467-761_4467-760del	XM_005270265.1:c.4467-760del	XM_005270265.1:c.4467-760dup	XM_005270265.1:c.4467-761_4467-760dup	XM_005270265.1:c.4467-762_4467-760dup	XM_005270265.1:c.4467-763_4467-760dup	XM_005270265.1:c.4467-764_4467-760dup	XM_005270265.1:c.4467-765_4467-760dup	XM_005270265.1:c.4467-767_4467-760dup	XM_005270265.1:c.4467-768_4467-760dup	XM_005270265.1:c.4467-769_4467-760dup	XM_005270265.1:c.4467-771_4467-760dup	XM_005270265.1:c.4467-773_4467-760dup	XM_005270265.1:c.4467-776_4467-760dup	XM_005270265.1:c.4467-760_4467-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X4	XM_005270266.1:c.4086-781=	XM_005270266.1:c.4086-773_4086-760del	XM_005270266.1:c.4086-772_4086-760del	XM_005270266.1:c.4086-771_4086-760del	XM_005270266.1:c.4086-770_4086-760del	XM_005270266.1:c.4086-769_4086-760del	XM_005270266.1:c.4086-767_4086-760del	XM_005270266.1:c.4086-766_4086-760del	XM_005270266.1:c.4086-764_4086-760del	XM_005270266.1:c.4086-762_4086-760del	XM_005270266.1:c.4086-761_4086-760del	XM_005270266.1:c.4086-760del	XM_005270266.1:c.4086-760dup	XM_005270266.1:c.4086-761_4086-760dup	XM_005270266.1:c.4086-762_4086-760dup	XM_005270266.1:c.4086-763_4086-760dup	XM_005270266.1:c.4086-764_4086-760dup	XM_005270266.1:c.4086-765_4086-760dup	XM_005270266.1:c.4086-767_4086-760dup	XM_005270266.1:c.4086-768_4086-760dup	XM_005270266.1:c.4086-769_4086-760dup	XM_005270266.1:c.4086-771_4086-760dup	XM_005270266.1:c.4086-773_4086-760dup	XM_005270266.1:c.4086-776_4086-760dup	XM_005270266.1:c.4086-760_4086-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X1	XM_011540326.3:c.4965-781=	XM_011540326.3:c.4965-773_4965-760del	XM_011540326.3:c.4965-772_4965-760del	XM_011540326.3:c.4965-771_4965-760del	XM_011540326.3:c.4965-770_4965-760del	XM_011540326.3:c.4965-769_4965-760del	XM_011540326.3:c.4965-767_4965-760del	XM_011540326.3:c.4965-766_4965-760del	XM_011540326.3:c.4965-764_4965-760del	XM_011540326.3:c.4965-762_4965-760del	XM_011540326.3:c.4965-761_4965-760del	XM_011540326.3:c.4965-760del	XM_011540326.3:c.4965-760dup	XM_011540326.3:c.4965-761_4965-760dup	XM_011540326.3:c.4965-762_4965-760dup	XM_011540326.3:c.4965-763_4965-760dup	XM_011540326.3:c.4965-764_4965-760dup	XM_011540326.3:c.4965-765_4965-760dup	XM_011540326.3:c.4965-767_4965-760dup	XM_011540326.3:c.4965-768_4965-760dup	XM_011540326.3:c.4965-769_4965-760dup	XM_011540326.3:c.4965-771_4965-760dup	XM_011540326.3:c.4965-773_4965-760dup	XM_011540326.3:c.4965-776_4965-760dup	XM_011540326.3:c.4965-760_4965-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X3	XM_011540327.3:c.4704-781=	XM_011540327.3:c.4704-773_4704-760del	XM_011540327.3:c.4704-772_4704-760del	XM_011540327.3:c.4704-771_4704-760del	XM_011540327.3:c.4704-770_4704-760del	XM_011540327.3:c.4704-769_4704-760del	XM_011540327.3:c.4704-767_4704-760del	XM_011540327.3:c.4704-766_4704-760del	XM_011540327.3:c.4704-764_4704-760del	XM_011540327.3:c.4704-762_4704-760del	XM_011540327.3:c.4704-761_4704-760del	XM_011540327.3:c.4704-760del	XM_011540327.3:c.4704-760dup	XM_011540327.3:c.4704-761_4704-760dup	XM_011540327.3:c.4704-762_4704-760dup	XM_011540327.3:c.4704-763_4704-760dup	XM_011540327.3:c.4704-764_4704-760dup	XM_011540327.3:c.4704-765_4704-760dup	XM_011540327.3:c.4704-767_4704-760dup	XM_011540327.3:c.4704-768_4704-760dup	XM_011540327.3:c.4704-769_4704-760dup	XM_011540327.3:c.4704-771_4704-760dup	XM_011540327.3:c.4704-773_4704-760dup	XM_011540327.3:c.4704-776_4704-760dup	XM_011540327.3:c.4704-760_4704-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X4	XM_011540328.3:c.4608-781=	XM_011540328.3:c.4608-773_4608-760del	XM_011540328.3:c.4608-772_4608-760del	XM_011540328.3:c.4608-771_4608-760del	XM_011540328.3:c.4608-770_4608-760del	XM_011540328.3:c.4608-769_4608-760del	XM_011540328.3:c.4608-767_4608-760del	XM_011540328.3:c.4608-766_4608-760del	XM_011540328.3:c.4608-764_4608-760del	XM_011540328.3:c.4608-762_4608-760del	XM_011540328.3:c.4608-761_4608-760del	XM_011540328.3:c.4608-760del	XM_011540328.3:c.4608-760dup	XM_011540328.3:c.4608-761_4608-760dup	XM_011540328.3:c.4608-762_4608-760dup	XM_011540328.3:c.4608-763_4608-760dup	XM_011540328.3:c.4608-764_4608-760dup	XM_011540328.3:c.4608-765_4608-760dup	XM_011540328.3:c.4608-767_4608-760dup	XM_011540328.3:c.4608-768_4608-760dup	XM_011540328.3:c.4608-769_4608-760dup	XM_011540328.3:c.4608-771_4608-760dup	XM_011540328.3:c.4608-773_4608-760dup	XM_011540328.3:c.4608-776_4608-760dup	XM_011540328.3:c.4608-760_4608-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X2	XM_017016877.2:c.4929-781=	XM_017016877.2:c.4929-773_4929-760del	XM_017016877.2:c.4929-772_4929-760del	XM_017016877.2:c.4929-771_4929-760del	XM_017016877.2:c.4929-770_4929-760del	XM_017016877.2:c.4929-769_4929-760del	XM_017016877.2:c.4929-767_4929-760del	XM_017016877.2:c.4929-766_4929-760del	XM_017016877.2:c.4929-764_4929-760del	XM_017016877.2:c.4929-762_4929-760del	XM_017016877.2:c.4929-761_4929-760del	XM_017016877.2:c.4929-760del	XM_017016877.2:c.4929-760dup	XM_017016877.2:c.4929-761_4929-760dup	XM_017016877.2:c.4929-762_4929-760dup	XM_017016877.2:c.4929-763_4929-760dup	XM_017016877.2:c.4929-764_4929-760dup	XM_017016877.2:c.4929-765_4929-760dup	XM_017016877.2:c.4929-767_4929-760dup	XM_017016877.2:c.4929-768_4929-760dup	XM_017016877.2:c.4929-769_4929-760dup	XM_017016877.2:c.4929-771_4929-760dup	XM_017016877.2:c.4929-773_4929-760dup	XM_017016877.2:c.4929-776_4929-760dup	XM_017016877.2:c.4929-760_4929-759insAAAAAAAAAAAAAAAAAAAAAAAAAA
BTAF1 transcript variant X5	XM_047425989.1:c.4086-781=	XM_047425989.1:c.4086-773_4086-760del	XM_047425989.1:c.4086-772_4086-760del	XM_047425989.1:c.4086-771_4086-760del	XM_047425989.1:c.4086-770_4086-760del	XM_047425989.1:c.4086-769_4086-760del	XM_047425989.1:c.4086-767_4086-760del	XM_047425989.1:c.4086-766_4086-760del	XM_047425989.1:c.4086-764_4086-760del	XM_047425989.1:c.4086-762_4086-760del	XM_047425989.1:c.4086-761_4086-760del	XM_047425989.1:c.4086-760del	XM_047425989.1:c.4086-760dup	XM_047425989.1:c.4086-761_4086-760dup	XM_047425989.1:c.4086-762_4086-760dup	XM_047425989.1:c.4086-763_4086-760dup	XM_047425989.1:c.4086-764_4086-760dup	XM_047425989.1:c.4086-765_4086-760dup	XM_047425989.1:c.4086-767_4086-760dup	XM_047425989.1:c.4086-768_4086-760dup	XM_047425989.1:c.4086-769_4086-760dup	XM_047425989.1:c.4086-771_4086-760dup	XM_047425989.1:c.4086-773_4086-760dup	XM_047425989.1:c.4086-776_4086-760dup	XM_047425989.1:c.4086-760_4086-759insAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

61 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95548927	Dec 05, 2013 (142)
2	PJP	ss294669773	May 09, 2011 (137)
3	PJP	ss294669774	May 09, 2011 (134)
4	EVA_UK10K_ALSPAC	ss1706848135	Apr 01, 2015 (144)
5	EVA_UK10K_TWINSUK	ss1706848594	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1710481348	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1710481398	Apr 01, 2015 (144)
8	SWEGEN	ss3006934727	Nov 08, 2017 (151)
9	URBANLAB	ss3649437336	Oct 12, 2018 (152)
10	EVA_DECODE	ss3690423973	Jul 13, 2019 (153)
11	EVA_DECODE	ss3690423974	Jul 13, 2019 (153)
12	EVA_DECODE	ss3690423975	Jul 13, 2019 (153)
13	EVA_DECODE	ss3690423976	Jul 13, 2019 (153)
14	EVA_DECODE	ss3690423977	Jul 13, 2019 (153)
15	EVA	ss3832266701	Apr 26, 2020 (154)
16	GNOMAD	ss4223298080	Apr 26, 2021 (155)
17	GNOMAD	ss4223298081	Apr 26, 2021 (155)
18	GNOMAD	ss4223298082	Apr 26, 2021 (155)
19	GNOMAD	ss4223298083	Apr 26, 2021 (155)
20	GNOMAD	ss4223298084	Apr 26, 2021 (155)
21	GNOMAD	ss4223298085	Apr 26, 2021 (155)
22	GNOMAD	ss4223298086	Apr 26, 2021 (155)
23	GNOMAD	ss4223298087	Apr 26, 2021 (155)
24	GNOMAD	ss4223298088	Apr 26, 2021 (155)
25	GNOMAD	ss4223298089	Apr 26, 2021 (155)
26	GNOMAD	ss4223298090	Apr 26, 2021 (155)
27	GNOMAD	ss4223298091	Apr 26, 2021 (155)
28	GNOMAD	ss4223298092	Apr 26, 2021 (155)
29	GNOMAD	ss4223298093	Apr 26, 2021 (155)
30	GNOMAD	ss4223298094	Apr 26, 2021 (155)
31	GNOMAD	ss4223298095	Apr 26, 2021 (155)
32	GNOMAD	ss4223298096	Apr 26, 2021 (155)
33	GNOMAD	ss4223298097	Apr 26, 2021 (155)
34	GNOMAD	ss4223298098	Apr 26, 2021 (155)
35	GNOMAD	ss4223298099	Apr 26, 2021 (155)
36	GNOMAD	ss4223298100	Apr 26, 2021 (155)
37	GNOMAD	ss4223298101	Apr 26, 2021 (155)
38	GNOMAD	ss4223298102	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5198883048	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5198883049	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5198883050	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5198883051	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5198883052	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5198883053	Apr 26, 2021 (155)
45	1000G_HIGH_COVERAGE	ss5285023420	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5285023421	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5285023422	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5285023423	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5285023425	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5480489436	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5480489437	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5480489438	Oct 16, 2022 (156)
53	HUGCELL_USP	ss5480489439	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5745073695	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5745073696	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5745073697	Oct 16, 2022 (156)
57	TOMMO_GENOMICS	ss5745073698	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5745073699	Oct 16, 2022 (156)
59	EVA	ss5824782544	Oct 16, 2022 (156)
60	EVA	ss5824782545	Oct 16, 2022 (156)
61	EVA	ss5880011985	Oct 16, 2022 (156)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28301532 (NC_000010.10:93785567::AA 2333/3854) Row 28301533 (NC_000010.10:93785567:AA: 1078/3854)	-	Oct 12, 2018 (152)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28301532 (NC_000010.10:93785567::AA 2333/3854) Row 28301533 (NC_000010.10:93785567:AA: 1078/3854)	-	Oct 12, 2018 (152)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 360189397 (NC_000010.11:92025810::A 27101/79896) Row 360189398 (NC_000010.11:92025810::AA 3749/79574) Row 360189399 (NC_000010.11:92025810::AAA 326/79722)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 56852355 (NC_000010.10:93785567:A: 4396/16396) Row 56852356 (NC_000010.10:93785567::A 2891/16396) Row 56852357 (NC_000010.10:93785567::AA 104/16396)...	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 78910799 (NC_000010.11:92025810:A: 9644/28114) Row 78910800 (NC_000010.11:92025810::A 5745/28114) Row 78910801 (NC_000010.11:92025810::AA 170/28114)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 78910799 (NC_000010.11:92025810:A: 9644/28114) Row 78910800 (NC_000010.11:92025810::A 5745/28114) Row 78910801 (NC_000010.11:92025810::AA 170/28114)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 78910799 (NC_000010.11:92025810:A: 9644/28114) Row 78910800 (NC_000010.11:92025810::A 5745/28114) Row 78910801 (NC_000010.11:92025810::AA 170/28114)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 78910799 (NC_000010.11:92025810:A: 9644/28114) Row 78910800 (NC_000010.11:92025810::A 5745/28114) Row 78910801 (NC_000010.11:92025810::AA 170/28114)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 78910799 (NC_000010.11:92025810:A: 9644/28114) Row 78910800 (NC_000010.11:92025810::A 5745/28114) Row 78910801 (NC_000010.11:92025810::AA 170/28114)...	-	Oct 16, 2022 (156)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28301532 (NC_000010.10:93785567::AA 2286/3708) Row 28301533 (NC_000010.10:93785567:AA: 972/3708)	-	Oct 12, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28301532 (NC_000010.10:93785567::AA 2286/3708) Row 28301533 (NC_000010.10:93785567:AA: 972/3708)	-	Oct 12, 2018 (152)
100	ALFA	NC_000010.11 - 92025811	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)
rs143379299	May 11, 2012 (137)
rs398014431	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4223298102	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4223298101	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4223298100	NC_000010.11:92025810:AAAAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4223298099	NC_000010.11:92025810:AAAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4223298098	NC_000010.11:92025810:AAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4223298097	NC_000010.11:92025810:AAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4223298096	NC_000010.11:92025810:AAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3690423977, ss4223298095	NC_000010.11:92025810:AAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1706848135, ss1706848594, ss3006934727, ss5198883051, ss5824782545	NC_000010.10:93785567:AA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4223298094, ss5285023425, ss5480489439, ss5745073698, ss5880011985	NC_000010.11:92025810:AA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3690423976	NC_000010.11:92025811:AA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294669773	NC_000010.9:93775547:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294669774	NC_000010.9:93775568:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3832266701, ss5198883048	NC_000010.10:93785567:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3649437336, ss4223298093, ss5285023420, ss5480489438, ss5745073695	NC_000010.11:92025810:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3690423975	NC_000010.11:92025812:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss95548927	NT_030059.13:44590052:A:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5198883049	NC_000010.10:93785567::A	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298080, ss5285023422, ss5480489436, ss5745073696	NC_000010.11:92025810::A	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690423974	NC_000010.11:92025813::A	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5198883050, ss5824782544	NC_000010.10:93785567::AA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss1710481348, ss1710481398	NC_000010.10:93785569::AA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298081, ss5285023421, ss5480489437, ss5745073697	NC_000010.11:92025810::AA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3690423973	NC_000010.11:92025813::AA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5198883052	NC_000010.10:93785567::AAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298082, ss5285023423, ss5745073699	NC_000010.11:92025810::AAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298083	NC_000010.11:92025810::AAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5198883053	NC_000010.10:93785567::AAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298084	NC_000010.11:92025810::AAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298085	NC_000010.11:92025810::AAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
6801433439	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298086	NC_000010.11:92025810::AAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298087	NC_000010.11:92025810::AAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298088	NC_000010.11:92025810::AAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298089	NC_000010.11:92025810::AAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298090	NC_000010.11:92025810::AAAAAAAAAAA… NC_000010.11:92025810::AAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298091	NC_000010.11:92025810::AAAAAAAAAAA… NC_000010.11:92025810::AAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4223298092	NC_000010.11:92025810::AAAAAAAAAAA… NC_000010.11:92025810::AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2340105391	NC_000010.10:93785567:AAAAAAAAAAAA:	NC_000010.11:92025810:AAAAAAAAAAAA… NC_000010.11:92025810:AAAAAAAAAAAAAAAAAAAAAA: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 rs71025383

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

rs71025383