Name: rs111697845
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.

rs111697845

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:102862329-102862345 (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)₇ / del(A)₅ / del(A)₄ / delA…
del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₇=0.0000 (0/6520, ALFA)
del(A)₄=0.0000 (0/6520, ALFA)
delAAA=0.0000 (0/6520, ALFA) (+ 7 more)
delAA=0.0000 (0/6520, ALFA)
delA=0.0000 (0/6520, ALFA)
dupA=0.0000 (0/6520, ALFA)
dupAA=0.0000 (0/6520, ALFA)
delAA=0.2055 (1029/5008, 1000G)
delAA=0.1204 (464/3854, ALSPAC)
delAA=0.1251 (464/3708, TWINSUK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXL13 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	6520	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	4742	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1014	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	30	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	984	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	18	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	92	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	372	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	44	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	238	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6520	(A)₁₇=1.0000	del(A)₇=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	4742	(A)₁₇=1.0000	del(A)₇=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	1014	(A)₁₇=1.0000	del(A)₇=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	372	(A)₁₇=1.000	del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	238	(A)₁₇=1.000	del(A)₇=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	92	(A)₁₇=1.00	del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	44	(A)₁₇=1.00	del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	18	(A)₁₇=1.00	del(A)₇=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.7945	delAA=0.2055
1000Genomes	African	Sub	1322	(A)₁₇=0.7731	delAA=0.2269
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.7242	delAA=0.2758
1000Genomes	Europe	Sub	1006	(A)₁₇=0.9006	delAA=0.0994
1000Genomes	South Asian	Sub	978	(A)₁₇=0.742	delAA=0.258
1000Genomes	American	Sub	694	(A)₁₇=0.857	delAA=0.143
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₇=0.8796	delAA=0.1204
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₇=0.8749	delAA=0.1251

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 7	NC_000007.14:g.102862339_102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862341_102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862342_102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862343_102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862344_102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862345del
GRCh38.p14 chr 7	NC_000007.14:g.102862345dup
GRCh38.p14 chr 7	NC_000007.14:g.102862344_102862345dup
GRCh38.p14 chr 7	NC_000007.14:g.102862343_102862345dup
GRCh38.p14 chr 7	NC_000007.14:g.102862342_102862345dup
GRCh38.p14 chr 7	NC_000007.14:g.102862341_102862345dup
GRCh38.p14 chr 7	NC_000007.14:g.102862340_102862345dup
GRCh37.p13 chr 7	NC_000007.13:g.102502786_102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502788_102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502789_102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502790_102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502791_102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502792del
GRCh37.p13 chr 7	NC_000007.13:g.102502792dup
GRCh37.p13 chr 7	NC_000007.13:g.102502791_102502792dup
GRCh37.p13 chr 7	NC_000007.13:g.102502790_102502792dup
GRCh37.p13 chr 7	NC_000007.13:g.102502789_102502792dup
GRCh37.p13 chr 7	NC_000007.13:g.102502788_102502792dup
GRCh37.p13 chr 7	NC_000007.13:g.102502787_102502792dup

Gene: FBXL13, F-box and leucine rich repeat protein 13 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXL13 transcript variant 2	NM_001111038.2:c.1636-747… NM_001111038.2:c.1636-7475_1636-7469del	N/A	Intron Variant
FBXL13 transcript variant 3	NM_001287150.2:c.1635+151… NM_001287150.2:c.1635+15132_1635+15138del	N/A	Intron Variant
FBXL13 transcript variant 5	NM_001394494.2:c.1906-747… NM_001394494.2:c.1906-7475_1906-7469del	N/A	Intron Variant
FBXL13 transcript variant 1	NM_145032.3:c.1636-7475_1… NM_145032.3:c.1636-7475_1636-7469del	N/A	Intron Variant
FBXL13 transcript variant 4	NR_105043.2:n.	N/A	Intron Variant
FBXL13 transcript variant X4	XM_005250207.5:c.1807-747… XM_005250207.5:c.1807-7475_1807-7469del	N/A	Intron Variant
FBXL13 transcript variant X6	XM_005250208.5:c.1906-747… XM_005250208.5:c.1906-7475_1906-7469del	N/A	Intron Variant
FBXL13 transcript variant X14	XM_006715898.4:c.1183-747… XM_006715898.4:c.1183-7475_1183-7469del	N/A	Intron Variant
FBXL13 transcript variant X3	XM_011515928.4:c.1905+151… XM_011515928.4:c.1905+15132_1905+15138del	N/A	Intron Variant
FBXL13 transcript variant X5	XM_011515929.4:c.1906-747… XM_011515929.4:c.1906-7475_1906-7469del	N/A	Intron Variant
FBXL13 transcript variant X10	XM_011515930.3:c.1636-747… XM_011515930.3:c.1636-7475_1636-7469del	N/A	Intron Variant
FBXL13 transcript variant X1	XM_017011850.3:c.1897-747… XM_017011850.3:c.1897-7475_1897-7469del	N/A	Intron Variant
FBXL13 transcript variant X2	XM_017011851.3:c.1906-747… XM_017011851.3:c.1906-7475_1906-7469del	N/A	Intron Variant
FBXL13 transcript variant X7	XM_017011852.2:c.1771-747… XM_017011852.2:c.1771-7475_1771-7469del	N/A	Intron Variant
FBXL13 transcript variant X9	XM_017011853.2:c.1636-747… XM_017011853.2:c.1636-7475_1636-7469del	N/A	Intron Variant
FBXL13 transcript variant X15	XM_024446687.2:c.1183-747… XM_024446687.2:c.1183-7475_1183-7469del	N/A	Intron Variant
FBXL13 transcript variant X8	XM_047420043.1:c.1906-747… XM_047420043.1:c.1906-7475_1906-7469del	N/A	Intron Variant
FBXL13 transcript variant X11	XM_047420044.1:c.1081-747… XM_047420044.1:c.1081-7475_1081-7469del	N/A	Intron Variant
FBXL13 transcript variant X16	XM_047420045.1:c.1084-747… XM_047420045.1:c.1084-7475_1084-7469del	N/A	Intron Variant
FBXL13 transcript variant X13	XM_011515932.4:c.	N/A	Genic Downstream Transcript Variant
FBXL13 transcript variant X12	XR_927410.4:n.	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)₁₇=	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆
GRCh38.p14 chr 7	NC_000007.14:g.102862329_102862345=	NC_000007.14:g.102862339_102862345del	NC_000007.14:g.102862341_102862345del	NC_000007.14:g.102862342_102862345del	NC_000007.14:g.102862343_102862345del	NC_000007.14:g.102862344_102862345del	NC_000007.14:g.102862345del	NC_000007.14:g.102862345dup	NC_000007.14:g.102862344_102862345dup	NC_000007.14:g.102862343_102862345dup	NC_000007.14:g.102862342_102862345dup	NC_000007.14:g.102862341_102862345dup	NC_000007.14:g.102862340_102862345dup
GRCh37.p13 chr 7	NC_000007.13:g.102502776_102502792=	NC_000007.13:g.102502786_102502792del	NC_000007.13:g.102502788_102502792del	NC_000007.13:g.102502789_102502792del	NC_000007.13:g.102502790_102502792del	NC_000007.13:g.102502791_102502792del	NC_000007.13:g.102502792del	NC_000007.13:g.102502792dup	NC_000007.13:g.102502791_102502792dup	NC_000007.13:g.102502790_102502792dup	NC_000007.13:g.102502789_102502792dup	NC_000007.13:g.102502788_102502792dup	NC_000007.13:g.102502787_102502792dup
FBXL13 transcript variant 2	NM_001111038.1:c.1636-7469=	NM_001111038.1:c.1636-7475_1636-7469del	NM_001111038.1:c.1636-7473_1636-7469del	NM_001111038.1:c.1636-7472_1636-7469del	NM_001111038.1:c.1636-7471_1636-7469del	NM_001111038.1:c.1636-7470_1636-7469del	NM_001111038.1:c.1636-7469del	NM_001111038.1:c.1636-7469dup	NM_001111038.1:c.1636-7470_1636-7469dup	NM_001111038.1:c.1636-7471_1636-7469dup	NM_001111038.1:c.1636-7472_1636-7469dup	NM_001111038.1:c.1636-7473_1636-7469dup	NM_001111038.1:c.1636-7474_1636-7469dup
FBXL13 transcript variant 2	NM_001111038.2:c.1636-7469=	NM_001111038.2:c.1636-7475_1636-7469del	NM_001111038.2:c.1636-7473_1636-7469del	NM_001111038.2:c.1636-7472_1636-7469del	NM_001111038.2:c.1636-7471_1636-7469del	NM_001111038.2:c.1636-7470_1636-7469del	NM_001111038.2:c.1636-7469del	NM_001111038.2:c.1636-7469dup	NM_001111038.2:c.1636-7470_1636-7469dup	NM_001111038.2:c.1636-7471_1636-7469dup	NM_001111038.2:c.1636-7472_1636-7469dup	NM_001111038.2:c.1636-7473_1636-7469dup	NM_001111038.2:c.1636-7474_1636-7469dup
FBXL13 transcript variant 3	NM_001287150.2:c.1635+15138=	NM_001287150.2:c.1635+15132_1635+15138del	NM_001287150.2:c.1635+15134_1635+15138del	NM_001287150.2:c.1635+15135_1635+15138del	NM_001287150.2:c.1635+15136_1635+15138del	NM_001287150.2:c.1635+15137_1635+15138del	NM_001287150.2:c.1635+15138del	NM_001287150.2:c.1635+15138dup	NM_001287150.2:c.1635+15137_1635+15138dup	NM_001287150.2:c.1635+15136_1635+15138dup	NM_001287150.2:c.1635+15135_1635+15138dup	NM_001287150.2:c.1635+15134_1635+15138dup	NM_001287150.2:c.1635+15133_1635+15138dup
FBXL13 transcript variant 5	NM_001394494.2:c.1906-7469=	NM_001394494.2:c.1906-7475_1906-7469del	NM_001394494.2:c.1906-7473_1906-7469del	NM_001394494.2:c.1906-7472_1906-7469del	NM_001394494.2:c.1906-7471_1906-7469del	NM_001394494.2:c.1906-7470_1906-7469del	NM_001394494.2:c.1906-7469del	NM_001394494.2:c.1906-7469dup	NM_001394494.2:c.1906-7470_1906-7469dup	NM_001394494.2:c.1906-7471_1906-7469dup	NM_001394494.2:c.1906-7472_1906-7469dup	NM_001394494.2:c.1906-7473_1906-7469dup	NM_001394494.2:c.1906-7474_1906-7469dup
FBXL13 transcript variant 1	NM_145032.3:c.1636-7469=	NM_145032.3:c.1636-7475_1636-7469del	NM_145032.3:c.1636-7473_1636-7469del	NM_145032.3:c.1636-7472_1636-7469del	NM_145032.3:c.1636-7471_1636-7469del	NM_145032.3:c.1636-7470_1636-7469del	NM_145032.3:c.1636-7469del	NM_145032.3:c.1636-7469dup	NM_145032.3:c.1636-7470_1636-7469dup	NM_145032.3:c.1636-7471_1636-7469dup	NM_145032.3:c.1636-7472_1636-7469dup	NM_145032.3:c.1636-7473_1636-7469dup	NM_145032.3:c.1636-7474_1636-7469dup
FBXL13 transcript variant X1	XM_005250205.1:c.1906-7469=	XM_005250205.1:c.1906-7475_1906-7469del	XM_005250205.1:c.1906-7473_1906-7469del	XM_005250205.1:c.1906-7472_1906-7469del	XM_005250205.1:c.1906-7471_1906-7469del	XM_005250205.1:c.1906-7470_1906-7469del	XM_005250205.1:c.1906-7469del	XM_005250205.1:c.1906-7469dup	XM_005250205.1:c.1906-7470_1906-7469dup	XM_005250205.1:c.1906-7471_1906-7469dup	XM_005250205.1:c.1906-7472_1906-7469dup	XM_005250205.1:c.1906-7473_1906-7469dup	XM_005250205.1:c.1906-7474_1906-7469dup
FBXL13 transcript variant X2	XM_005250206.1:c.1905+15138=	XM_005250206.1:c.1905+15132_1905+15138del	XM_005250206.1:c.1905+15134_1905+15138del	XM_005250206.1:c.1905+15135_1905+15138del	XM_005250206.1:c.1905+15136_1905+15138del	XM_005250206.1:c.1905+15137_1905+15138del	XM_005250206.1:c.1905+15138del	XM_005250206.1:c.1905+15138dup	XM_005250206.1:c.1905+15137_1905+15138dup	XM_005250206.1:c.1905+15136_1905+15138dup	XM_005250206.1:c.1905+15135_1905+15138dup	XM_005250206.1:c.1905+15134_1905+15138dup	XM_005250206.1:c.1905+15133_1905+15138dup
FBXL13 transcript variant X3	XM_005250207.1:c.1807-7469=	XM_005250207.1:c.1807-7475_1807-7469del	XM_005250207.1:c.1807-7473_1807-7469del	XM_005250207.1:c.1807-7472_1807-7469del	XM_005250207.1:c.1807-7471_1807-7469del	XM_005250207.1:c.1807-7470_1807-7469del	XM_005250207.1:c.1807-7469del	XM_005250207.1:c.1807-7469dup	XM_005250207.1:c.1807-7470_1807-7469dup	XM_005250207.1:c.1807-7471_1807-7469dup	XM_005250207.1:c.1807-7472_1807-7469dup	XM_005250207.1:c.1807-7473_1807-7469dup	XM_005250207.1:c.1807-7474_1807-7469dup
FBXL13 transcript variant X4	XM_005250207.5:c.1807-7469=	XM_005250207.5:c.1807-7475_1807-7469del	XM_005250207.5:c.1807-7473_1807-7469del	XM_005250207.5:c.1807-7472_1807-7469del	XM_005250207.5:c.1807-7471_1807-7469del	XM_005250207.5:c.1807-7470_1807-7469del	XM_005250207.5:c.1807-7469del	XM_005250207.5:c.1807-7469dup	XM_005250207.5:c.1807-7470_1807-7469dup	XM_005250207.5:c.1807-7471_1807-7469dup	XM_005250207.5:c.1807-7472_1807-7469dup	XM_005250207.5:c.1807-7473_1807-7469dup	XM_005250207.5:c.1807-7474_1807-7469dup
FBXL13 transcript variant X4	XM_005250208.1:c.1906-7469=	XM_005250208.1:c.1906-7475_1906-7469del	XM_005250208.1:c.1906-7473_1906-7469del	XM_005250208.1:c.1906-7472_1906-7469del	XM_005250208.1:c.1906-7471_1906-7469del	XM_005250208.1:c.1906-7470_1906-7469del	XM_005250208.1:c.1906-7469del	XM_005250208.1:c.1906-7469dup	XM_005250208.1:c.1906-7470_1906-7469dup	XM_005250208.1:c.1906-7471_1906-7469dup	XM_005250208.1:c.1906-7472_1906-7469dup	XM_005250208.1:c.1906-7473_1906-7469dup	XM_005250208.1:c.1906-7474_1906-7469dup
FBXL13 transcript variant X6	XM_005250208.5:c.1906-7469=	XM_005250208.5:c.1906-7475_1906-7469del	XM_005250208.5:c.1906-7473_1906-7469del	XM_005250208.5:c.1906-7472_1906-7469del	XM_005250208.5:c.1906-7471_1906-7469del	XM_005250208.5:c.1906-7470_1906-7469del	XM_005250208.5:c.1906-7469del	XM_005250208.5:c.1906-7469dup	XM_005250208.5:c.1906-7470_1906-7469dup	XM_005250208.5:c.1906-7471_1906-7469dup	XM_005250208.5:c.1906-7472_1906-7469dup	XM_005250208.5:c.1906-7473_1906-7469dup	XM_005250208.5:c.1906-7474_1906-7469dup
FBXL13 transcript variant X9	XM_005250209.1:c.1636-7469=	XM_005250209.1:c.1636-7475_1636-7469del	XM_005250209.1:c.1636-7473_1636-7469del	XM_005250209.1:c.1636-7472_1636-7469del	XM_005250209.1:c.1636-7471_1636-7469del	XM_005250209.1:c.1636-7470_1636-7469del	XM_005250209.1:c.1636-7469del	XM_005250209.1:c.1636-7469dup	XM_005250209.1:c.1636-7470_1636-7469dup	XM_005250209.1:c.1636-7471_1636-7469dup	XM_005250209.1:c.1636-7472_1636-7469dup	XM_005250209.1:c.1636-7473_1636-7469dup	XM_005250209.1:c.1636-7474_1636-7469dup
FBXL13 transcript variant X6	XM_005250210.1:c.1635+15138=	XM_005250210.1:c.1635+15132_1635+15138del	XM_005250210.1:c.1635+15134_1635+15138del	XM_005250210.1:c.1635+15135_1635+15138del	XM_005250210.1:c.1635+15136_1635+15138del	XM_005250210.1:c.1635+15137_1635+15138del	XM_005250210.1:c.1635+15138del	XM_005250210.1:c.1635+15138dup	XM_005250210.1:c.1635+15137_1635+15138dup	XM_005250210.1:c.1635+15136_1635+15138dup	XM_005250210.1:c.1635+15135_1635+15138dup	XM_005250210.1:c.1635+15134_1635+15138dup	XM_005250210.1:c.1635+15133_1635+15138dup
FBXL13 transcript variant X8	XM_005250212.1:c.1279-40126=	XM_005250212.1:c.1279-40132_1279-40126del	XM_005250212.1:c.1279-40130_1279-40126del	XM_005250212.1:c.1279-40129_1279-40126del	XM_005250212.1:c.1279-40128_1279-40126del	XM_005250212.1:c.1279-40127_1279-40126del	XM_005250212.1:c.1279-40126del	XM_005250212.1:c.1279-40126dup	XM_005250212.1:c.1279-40127_1279-40126dup	XM_005250212.1:c.1279-40128_1279-40126dup	XM_005250212.1:c.1279-40129_1279-40126dup	XM_005250212.1:c.1279-40130_1279-40126dup	XM_005250212.1:c.1279-40131_1279-40126dup
FBXL13 transcript variant X9	XM_005250213.1:c.1009-40126=	XM_005250213.1:c.1009-40132_1009-40126del	XM_005250213.1:c.1009-40130_1009-40126del	XM_005250213.1:c.1009-40129_1009-40126del	XM_005250213.1:c.1009-40128_1009-40126del	XM_005250213.1:c.1009-40127_1009-40126del	XM_005250213.1:c.1009-40126del	XM_005250213.1:c.1009-40126dup	XM_005250213.1:c.1009-40127_1009-40126dup	XM_005250213.1:c.1009-40128_1009-40126dup	XM_005250213.1:c.1009-40129_1009-40126dup	XM_005250213.1:c.1009-40130_1009-40126dup	XM_005250213.1:c.1009-40131_1009-40126dup
FBXL13 transcript variant X14	XM_006715898.4:c.1183-7469=	XM_006715898.4:c.1183-7475_1183-7469del	XM_006715898.4:c.1183-7473_1183-7469del	XM_006715898.4:c.1183-7472_1183-7469del	XM_006715898.4:c.1183-7471_1183-7469del	XM_006715898.4:c.1183-7470_1183-7469del	XM_006715898.4:c.1183-7469del	XM_006715898.4:c.1183-7469dup	XM_006715898.4:c.1183-7470_1183-7469dup	XM_006715898.4:c.1183-7471_1183-7469dup	XM_006715898.4:c.1183-7472_1183-7469dup	XM_006715898.4:c.1183-7473_1183-7469dup	XM_006715898.4:c.1183-7474_1183-7469dup
FBXL13 transcript variant X3	XM_011515928.4:c.1905+15138=	XM_011515928.4:c.1905+15132_1905+15138del	XM_011515928.4:c.1905+15134_1905+15138del	XM_011515928.4:c.1905+15135_1905+15138del	XM_011515928.4:c.1905+15136_1905+15138del	XM_011515928.4:c.1905+15137_1905+15138del	XM_011515928.4:c.1905+15138del	XM_011515928.4:c.1905+15138dup	XM_011515928.4:c.1905+15137_1905+15138dup	XM_011515928.4:c.1905+15136_1905+15138dup	XM_011515928.4:c.1905+15135_1905+15138dup	XM_011515928.4:c.1905+15134_1905+15138dup	XM_011515928.4:c.1905+15133_1905+15138dup
FBXL13 transcript variant X5	XM_011515929.4:c.1906-7469=	XM_011515929.4:c.1906-7475_1906-7469del	XM_011515929.4:c.1906-7473_1906-7469del	XM_011515929.4:c.1906-7472_1906-7469del	XM_011515929.4:c.1906-7471_1906-7469del	XM_011515929.4:c.1906-7470_1906-7469del	XM_011515929.4:c.1906-7469del	XM_011515929.4:c.1906-7469dup	XM_011515929.4:c.1906-7470_1906-7469dup	XM_011515929.4:c.1906-7471_1906-7469dup	XM_011515929.4:c.1906-7472_1906-7469dup	XM_011515929.4:c.1906-7473_1906-7469dup	XM_011515929.4:c.1906-7474_1906-7469dup
FBXL13 transcript variant X10	XM_011515930.3:c.1636-7469=	XM_011515930.3:c.1636-7475_1636-7469del	XM_011515930.3:c.1636-7473_1636-7469del	XM_011515930.3:c.1636-7472_1636-7469del	XM_011515930.3:c.1636-7471_1636-7469del	XM_011515930.3:c.1636-7470_1636-7469del	XM_011515930.3:c.1636-7469del	XM_011515930.3:c.1636-7469dup	XM_011515930.3:c.1636-7470_1636-7469dup	XM_011515930.3:c.1636-7471_1636-7469dup	XM_011515930.3:c.1636-7472_1636-7469dup	XM_011515930.3:c.1636-7473_1636-7469dup	XM_011515930.3:c.1636-7474_1636-7469dup
FBXL13 transcript variant X1	XM_017011850.3:c.1897-7469=	XM_017011850.3:c.1897-7475_1897-7469del	XM_017011850.3:c.1897-7473_1897-7469del	XM_017011850.3:c.1897-7472_1897-7469del	XM_017011850.3:c.1897-7471_1897-7469del	XM_017011850.3:c.1897-7470_1897-7469del	XM_017011850.3:c.1897-7469del	XM_017011850.3:c.1897-7469dup	XM_017011850.3:c.1897-7470_1897-7469dup	XM_017011850.3:c.1897-7471_1897-7469dup	XM_017011850.3:c.1897-7472_1897-7469dup	XM_017011850.3:c.1897-7473_1897-7469dup	XM_017011850.3:c.1897-7474_1897-7469dup
FBXL13 transcript variant X2	XM_017011851.3:c.1906-7469=	XM_017011851.3:c.1906-7475_1906-7469del	XM_017011851.3:c.1906-7473_1906-7469del	XM_017011851.3:c.1906-7472_1906-7469del	XM_017011851.3:c.1906-7471_1906-7469del	XM_017011851.3:c.1906-7470_1906-7469del	XM_017011851.3:c.1906-7469del	XM_017011851.3:c.1906-7469dup	XM_017011851.3:c.1906-7470_1906-7469dup	XM_017011851.3:c.1906-7471_1906-7469dup	XM_017011851.3:c.1906-7472_1906-7469dup	XM_017011851.3:c.1906-7473_1906-7469dup	XM_017011851.3:c.1906-7474_1906-7469dup
FBXL13 transcript variant X7	XM_017011852.2:c.1771-7469=	XM_017011852.2:c.1771-7475_1771-7469del	XM_017011852.2:c.1771-7473_1771-7469del	XM_017011852.2:c.1771-7472_1771-7469del	XM_017011852.2:c.1771-7471_1771-7469del	XM_017011852.2:c.1771-7470_1771-7469del	XM_017011852.2:c.1771-7469del	XM_017011852.2:c.1771-7469dup	XM_017011852.2:c.1771-7470_1771-7469dup	XM_017011852.2:c.1771-7471_1771-7469dup	XM_017011852.2:c.1771-7472_1771-7469dup	XM_017011852.2:c.1771-7473_1771-7469dup	XM_017011852.2:c.1771-7474_1771-7469dup
FBXL13 transcript variant X9	XM_017011853.2:c.1636-7469=	XM_017011853.2:c.1636-7475_1636-7469del	XM_017011853.2:c.1636-7473_1636-7469del	XM_017011853.2:c.1636-7472_1636-7469del	XM_017011853.2:c.1636-7471_1636-7469del	XM_017011853.2:c.1636-7470_1636-7469del	XM_017011853.2:c.1636-7469del	XM_017011853.2:c.1636-7469dup	XM_017011853.2:c.1636-7470_1636-7469dup	XM_017011853.2:c.1636-7471_1636-7469dup	XM_017011853.2:c.1636-7472_1636-7469dup	XM_017011853.2:c.1636-7473_1636-7469dup	XM_017011853.2:c.1636-7474_1636-7469dup
FBXL13 transcript variant X15	XM_024446687.2:c.1183-7469=	XM_024446687.2:c.1183-7475_1183-7469del	XM_024446687.2:c.1183-7473_1183-7469del	XM_024446687.2:c.1183-7472_1183-7469del	XM_024446687.2:c.1183-7471_1183-7469del	XM_024446687.2:c.1183-7470_1183-7469del	XM_024446687.2:c.1183-7469del	XM_024446687.2:c.1183-7469dup	XM_024446687.2:c.1183-7470_1183-7469dup	XM_024446687.2:c.1183-7471_1183-7469dup	XM_024446687.2:c.1183-7472_1183-7469dup	XM_024446687.2:c.1183-7473_1183-7469dup	XM_024446687.2:c.1183-7474_1183-7469dup
FBXL13 transcript variant X8	XM_047420043.1:c.1906-7469=	XM_047420043.1:c.1906-7475_1906-7469del	XM_047420043.1:c.1906-7473_1906-7469del	XM_047420043.1:c.1906-7472_1906-7469del	XM_047420043.1:c.1906-7471_1906-7469del	XM_047420043.1:c.1906-7470_1906-7469del	XM_047420043.1:c.1906-7469del	XM_047420043.1:c.1906-7469dup	XM_047420043.1:c.1906-7470_1906-7469dup	XM_047420043.1:c.1906-7471_1906-7469dup	XM_047420043.1:c.1906-7472_1906-7469dup	XM_047420043.1:c.1906-7473_1906-7469dup	XM_047420043.1:c.1906-7474_1906-7469dup
FBXL13 transcript variant X11	XM_047420044.1:c.1081-7469=	XM_047420044.1:c.1081-7475_1081-7469del	XM_047420044.1:c.1081-7473_1081-7469del	XM_047420044.1:c.1081-7472_1081-7469del	XM_047420044.1:c.1081-7471_1081-7469del	XM_047420044.1:c.1081-7470_1081-7469del	XM_047420044.1:c.1081-7469del	XM_047420044.1:c.1081-7469dup	XM_047420044.1:c.1081-7470_1081-7469dup	XM_047420044.1:c.1081-7471_1081-7469dup	XM_047420044.1:c.1081-7472_1081-7469dup	XM_047420044.1:c.1081-7473_1081-7469dup	XM_047420044.1:c.1081-7474_1081-7469dup
FBXL13 transcript variant X16	XM_047420045.1:c.1084-7469=	XM_047420045.1:c.1084-7475_1084-7469del	XM_047420045.1:c.1084-7473_1084-7469del	XM_047420045.1:c.1084-7472_1084-7469del	XM_047420045.1:c.1084-7471_1084-7469del	XM_047420045.1:c.1084-7470_1084-7469del	XM_047420045.1:c.1084-7469del	XM_047420045.1:c.1084-7469dup	XM_047420045.1:c.1084-7470_1084-7469dup	XM_047420045.1:c.1084-7471_1084-7469dup	XM_047420045.1:c.1084-7472_1084-7469dup	XM_047420045.1:c.1084-7473_1084-7469dup	XM_047420045.1:c.1084-7474_1084-7469dup

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#.

48 SubSNP, 26 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193937288	Jul 04, 2010 (132)
2	GMI	ss288862117	May 04, 2012 (137)
3	SSIP	ss947202928	Aug 21, 2014 (142)
4	1000GENOMES	ss1377464721	Aug 21, 2014 (142)
5	EVA_UK10K_ALSPAC	ss1705758147	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1705758192	Apr 01, 2015 (144)
7	SYSTEMSBIOZJU	ss2626800998	Nov 08, 2017 (151)
8	EVA_DECODE	ss3720346554	Jul 13, 2019 (153)
9	EVA_DECODE	ss3720346555	Jul 13, 2019 (153)
10	EVA_DECODE	ss3720346556	Jul 13, 2019 (153)
11	EVA_DECODE	ss3720346557	Jul 13, 2019 (153)
12	EVA_DECODE	ss3720346558	Jul 13, 2019 (153)
13	EVA_DECODE	ss3720346559	Jul 13, 2019 (153)
14	ACPOP	ss3734921229	Jul 13, 2019 (153)
15	ACPOP	ss3734921230	Jul 13, 2019 (153)
16	ACPOP	ss3734921231	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3810120162	Jul 13, 2019 (153)
18	EVA	ss3830732820	Apr 26, 2020 (154)
19	GNOMAD	ss4169828819	Apr 26, 2021 (155)
20	GNOMAD	ss4169828820	Apr 26, 2021 (155)
21	GNOMAD	ss4169828821	Apr 26, 2021 (155)
22	GNOMAD	ss4169828822	Apr 26, 2021 (155)
23	GNOMAD	ss4169828823	Apr 26, 2021 (155)
24	GNOMAD	ss4169828824	Apr 26, 2021 (155)
25	GNOMAD	ss4169828825	Apr 26, 2021 (155)
26	GNOMAD	ss4169828826	Apr 26, 2021 (155)
27	GNOMAD	ss4169828827	Apr 26, 2021 (155)
28	GNOMAD	ss4169828828	Apr 26, 2021 (155)
29	GNOMAD	ss4169828829	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5184781232	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5184781233	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5184781234	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5184781235	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5274116504	Oct 15, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5274116505	Oct 15, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5274116507	Oct 15, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5274116508	Oct 15, 2022 (156)
38	HUGCELL_USP	ss5471069487	Oct 15, 2022 (156)
39	HUGCELL_USP	ss5471069488	Oct 15, 2022 (156)
40	HUGCELL_USP	ss5471069490	Oct 15, 2022 (156)
41	HUGCELL_USP	ss5471069491	Oct 15, 2022 (156)
42	TOMMO_GENOMICS	ss5725538929	Oct 15, 2022 (156)
43	TOMMO_GENOMICS	ss5725538930	Oct 15, 2022 (156)
44	TOMMO_GENOMICS	ss5725538931	Oct 15, 2022 (156)
45	TOMMO_GENOMICS	ss5725538933	Oct 15, 2022 (156)
46	EVA	ss5823286677	Oct 15, 2022 (156)
47	EVA	ss5823286678	Oct 15, 2022 (156)
48	EVA	ss5972811859	Oct 15, 2022 (156)
49	1000Genomes	NC_000007.13 - 102502776	Oct 12, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children	NC_000007.13 - 102502776	Oct 12, 2018 (152)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271309558 (NC_000007.14:102862328::A 781/88290) Row 271309559 (NC_000007.14:102862328::AA 3/88490) Row 271309560 (NC_000007.14:102862328::AAA 1/88492)...	-	Apr 26, 2021 (155)
62	Northern Sweden Submission ignored due to conflicting rows: Row 8206094 (NC_000007.13:102502775:A: 20/532) Row 8206095 (NC_000007.13:102502775:AA: 21/532) Row 8206096 (NC_000007.13:102502775:AAA: 19/532)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 8206094 (NC_000007.13:102502775:A: 20/532) Row 8206095 (NC_000007.13:102502775:AA: 21/532) Row 8206096 (NC_000007.13:102502775:AAA: 19/532)	-	Jul 13, 2019 (153)
64	Northern Sweden Submission ignored due to conflicting rows: Row 8206094 (NC_000007.13:102502775:A: 20/532) Row 8206095 (NC_000007.13:102502775:AA: 21/532) Row 8206096 (NC_000007.13:102502775:AAA: 19/532)	-	Jul 13, 2019 (153)
65	8.3KJPN Submission ignored due to conflicting rows: Row 42750539 (NC_000007.13:102502775:A: 4081/16716) Row 42750540 (NC_000007.13:102502775:AAA: 2080/16716) Row 42750541 (NC_000007.13:102502775:AA: 2725/16716)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 42750539 (NC_000007.13:102502775:A: 4081/16716) Row 42750540 (NC_000007.13:102502775:AAA: 2080/16716) Row 42750541 (NC_000007.13:102502775:AA: 2725/16716)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 42750539 (NC_000007.13:102502775:A: 4081/16716) Row 42750540 (NC_000007.13:102502775:AAA: 2080/16716) Row 42750541 (NC_000007.13:102502775:AA: 2725/16716)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 42750539 (NC_000007.13:102502775:A: 4081/16716) Row 42750540 (NC_000007.13:102502775:AAA: 2080/16716) Row 42750541 (NC_000007.13:102502775:AA: 2725/16716)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 59376033 (NC_000007.14:102862328:A: 7159/28254) Row 59376034 (NC_000007.14:102862328:AA: 4746/28254) Row 59376035 (NC_000007.14:102862328:AAA: 3557/28254)...	-	Oct 15, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 59376033 (NC_000007.14:102862328:A: 7159/28254) Row 59376034 (NC_000007.14:102862328:AA: 4746/28254) Row 59376035 (NC_000007.14:102862328:AAA: 3557/28254)...	-	Oct 15, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 59376033 (NC_000007.14:102862328:A: 7159/28254) Row 59376034 (NC_000007.14:102862328:AA: 4746/28254) Row 59376035 (NC_000007.14:102862328:AAA: 3557/28254)...	-	Oct 15, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 59376033 (NC_000007.14:102862328:A: 7159/28254) Row 59376034 (NC_000007.14:102862328:AA: 4746/28254) Row 59376035 (NC_000007.14:102862328:AAA: 3557/28254)...	-	Oct 15, 2022 (156)
73	UK 10K study - Twins	NC_000007.13 - 102502776	Oct 12, 2018 (152)
74	ALFA	NC_000007.14 - 102862329	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4169828829	NC_000007.14:102862328:AAAAAAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4169828828	NC_000007.14:102862328:AAAAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3720346559, ss4169828827	NC_000007.14:102862328:AAAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3734921231, ss5184781233, ss5823286677	NC_000007.13:102502775:AAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4169828826, ss5274116507, ss5471069491, ss5725538931	NC_000007.14:102862328:AAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3720346558	NC_000007.14:102862329:AAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
38439562, 21384131, 21384131, ss947202928, ss1377464721, ss1705758147, ss1705758192, ss3734921230, ss5184781234, ss5823286678, ss5972811859	NC_000007.13:102502775:AA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3810120162, ss4169828825, ss5274116504, ss5471069487, ss5725538930	NC_000007.14:102862328:AA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3720346557	NC_000007.14:102862330:AA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss288862117	NC_000007.12:102290011:A:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss2626800998, ss3734921229, ss3830732820, ss5184781232	NC_000007.13:102502775:A:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4169828824, ss5274116505, ss5471069488, ss5725538929	NC_000007.14:102862328:A:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3720346556	NC_000007.14:102862331:A:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss193937288	NT_007933.16:40355549:A:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5184781235	NC_000007.13:102502775::A	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4169828819, ss5274116508, ss5471069490, ss5725538933	NC_000007.14:102862328::A	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3720346555	NC_000007.14:102862332::A	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4169828820	NC_000007.14:102862328::AA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
9602278398	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4169828821	NC_000007.14:102862328::AAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3720346554	NC_000007.14:102862332::AAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4169828822	NC_000007.14:102862328::AAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4169828823	NC_000007.14:102862328::AAAAAA	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2465776915	NC_000007.13:102502775:AAAAAAA:	NC_000007.14:102862328:AAAAAAAAAAA… NC_000007.14:102862328:AAAAAAAAAAAAAAAAA: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 rs111697845

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

rs111697845