Name: rs35647787
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.

rs35647787

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:200610510-200610530 (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)₁₀ / del(A)₈ / del(A)₆ / del…
del(A)₁₀ / del(A)₈ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAAA / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupAAA=0.000004 (1/264690, TOPMED)
(A)₂₁=0.3988 (1997/5008, 1000G)
(A)₂₁=0.3919 (1806/4608, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: KIF14 : 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	Alt HMOZ	HTRZ	HWEP
Total	Global	4608	AAAAAAAAAAAAAAAAAAAAA=0.3919	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0004, AAAAAAAAAAAAAAAAAAA=0.1424, AAAAAAAAAAAAAAAAAAAA=0.4653, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.210993	0.283688	0.505319	0
European	Sub	4498	AAAAAAAAAAAAAAAAAAAAA=0.3784	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0004, AAAAAAAAAAAAAAAAAAA=0.1454, AAAAAAAAAAAAAAAAAAAA=0.4758, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	0.186699	0.292251	0.521049	3
African	Sub	70	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	70	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	16	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	12	AAAAAAAAAAAAAAAAAAAAA=0.50	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.17, AAAAAAAAAAAAAAAAAAAA=0.33, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	0.5	0.25	0.25	1

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	- No frequency provided	dupAAA=0.000004
1000Genomes	Global	Study-wide	5008	(A)₂₁=0.3988	delA=0.6012
1000Genomes	African	Sub	1322	(A)₂₁=0.4244	delA=0.5756
1000Genomes	East Asian	Sub	1008	(A)₂₁=0.4315	delA=0.5685
1000Genomes	Europe	Sub	1006	(A)₂₁=0.3549	delA=0.6451
1000Genomes	South Asian	Sub	978	(A)₂₁=0.422	delA=0.578
1000Genomes	American	Sub	694	(A)₂₁=0.333	delA=0.667
Allele Frequency Aggregator	Total	Global	4608	(A)₂₁=0.3919	del(A)₈=0.0000, del(A)₄=0.0000, delAAA=0.0004, delAA=0.1424, delA=0.4653, dupA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	4498	(A)₂₁=0.3784	del(A)₈=0.0000, del(A)₄=0.0000, delAAA=0.0004, delAA=0.1454, delA=0.4758, dupA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	70	(A)₂₁=1.00	del(A)₈=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	16	(A)₂₁=1.00	del(A)₈=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Other	Sub	12	(A)₂₁=0.50	del(A)₈=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.17, delA=0.33, dupA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₂₁=1.0	del(A)₈=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAAA=0.0
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₁=1.0	del(A)₈=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAAA=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₂₁=0	del(A)₈=0, del(A)₄=0, delAAA=0, delAA=0, delA=0, dupA=0, dupAAA=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 1	NC_000001.11:g.200610521_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610523_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610525_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610526_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610527_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610528_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610529_200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610530del
GRCh38.p14 chr 1	NC_000001.11:g.200610530dup
GRCh38.p14 chr 1	NC_000001.11:g.200610528_200610530dup
GRCh38.p14 chr 1	NC_000001.11:g.200610523_200610530dup
GRCh37.p13 chr 1	NC_000001.10:g.200579649_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579651_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579653_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579654_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579655_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579656_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579657_200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579658del
GRCh37.p13 chr 1	NC_000001.10:g.200579658dup
GRCh37.p13 chr 1	NC_000001.10:g.200579656_200579658dup
GRCh37.p13 chr 1	NC_000001.10:g.200579651_200579658dup
KIF14 RefSeqGene	NG_042074.1:g.15216_15225del
KIF14 RefSeqGene	NG_042074.1:g.15218_15225del
KIF14 RefSeqGene	NG_042074.1:g.15220_15225del
KIF14 RefSeqGene	NG_042074.1:g.15221_15225del
KIF14 RefSeqGene	NG_042074.1:g.15222_15225del
KIF14 RefSeqGene	NG_042074.1:g.15223_15225del
KIF14 RefSeqGene	NG_042074.1:g.15224_15225del
KIF14 RefSeqGene	NG_042074.1:g.15225del
KIF14 RefSeqGene	NG_042074.1:g.15225dup
KIF14 RefSeqGene	NG_042074.1:g.15223_15225dup
KIF14 RefSeqGene	NG_042074.1:g.15218_15225dup

Gene: KIF14, kinesin family member 14 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
KIF14 transcript variant 2	NM_001305792.1:c.-18-1591… NM_001305792.1:c.-18-1591_-18-1582del	N/A	Intron Variant
KIF14 transcript variant 1	NM_014875.3:c.1456-1591_1… NM_014875.3:c.1456-1591_1456-1582del	N/A	Intron Variant
KIF14 transcript variant X1	XM_011510231.3:c.1456-159… XM_011510231.3:c.1456-1591_1456-1582del	N/A	Intron Variant
KIF14 transcript variant X2	XM_011510232.3:c.1456-159… XM_011510232.3:c.1456-1591_1456-1582del	N/A	Intron Variant
KIF14 transcript variant X3	XM_011510233.3:c.1372-159… XM_011510233.3:c.1372-1591_1372-1582del	N/A	Intron Variant
KIF14 transcript variant X9	XM_011510235.3:c.1084-159… XM_011510235.3:c.1084-1591_1084-1582del	N/A	Intron Variant
KIF14 transcript variant X7	XM_017003006.2:c.1327-159… XM_017003006.2:c.1327-1591_1327-1582del	N/A	Intron Variant
KIF14 transcript variant X13	XM_017003007.2:c.889-1591… XM_017003007.2:c.889-1591_889-1582del	N/A	Intron Variant
KIF14 transcript variant X4	XM_047436181.1:c.1372-159… XM_047436181.1:c.1372-1591_1372-1582del	N/A	Intron Variant
KIF14 transcript variant X5	XM_047436184.1:c.1372-159… XM_047436184.1:c.1372-1591_1372-1582del	N/A	Intron Variant
KIF14 transcript variant X6	XM_047436190.1:c.1372-159… XM_047436190.1:c.1372-1591_1372-1582del	N/A	Intron Variant
KIF14 transcript variant X8	XM_047436195.1:c.1243-159… XM_047436195.1:c.1243-1591_1243-1582del	N/A	Intron Variant
KIF14 transcript variant X10	XM_047436197.1:c.1084-159… XM_047436197.1:c.1084-1591_1084-1582del	N/A	Intron Variant
KIF14 transcript variant X11	XM_047436198.1:c.1084-159… XM_047436198.1:c.1084-1591_1084-1582del	N/A	Intron Variant
KIF14 transcript variant X12	XM_047436199.1:c.955-1591… XM_047436199.1:c.955-1591_955-1582del	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)₂₁=	del(A)₁₀	del(A)₈	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAAA	dup(A)₈
GRCh38.p14 chr 1	NC_000001.11:g.200610510_200610530=	NC_000001.11:g.200610521_200610530del	NC_000001.11:g.200610523_200610530del	NC_000001.11:g.200610525_200610530del	NC_000001.11:g.200610526_200610530del	NC_000001.11:g.200610527_200610530del	NC_000001.11:g.200610528_200610530del	NC_000001.11:g.200610529_200610530del	NC_000001.11:g.200610530del	NC_000001.11:g.200610530dup	NC_000001.11:g.200610528_200610530dup	NC_000001.11:g.200610523_200610530dup
GRCh37.p13 chr 1	NC_000001.10:g.200579638_200579658=	NC_000001.10:g.200579649_200579658del	NC_000001.10:g.200579651_200579658del	NC_000001.10:g.200579653_200579658del	NC_000001.10:g.200579654_200579658del	NC_000001.10:g.200579655_200579658del	NC_000001.10:g.200579656_200579658del	NC_000001.10:g.200579657_200579658del	NC_000001.10:g.200579658del	NC_000001.10:g.200579658dup	NC_000001.10:g.200579656_200579658dup	NC_000001.10:g.200579651_200579658dup
KIF14 RefSeqGene	NG_042074.1:g.15205_15225=	NG_042074.1:g.15216_15225del	NG_042074.1:g.15218_15225del	NG_042074.1:g.15220_15225del	NG_042074.1:g.15221_15225del	NG_042074.1:g.15222_15225del	NG_042074.1:g.15223_15225del	NG_042074.1:g.15224_15225del	NG_042074.1:g.15225del	NG_042074.1:g.15225dup	NG_042074.1:g.15223_15225dup	NG_042074.1:g.15218_15225dup
KIF14 transcript variant 2	NM_001305792.1:c.-18-1582=	NM_001305792.1:c.-18-1591_-18-1582del	NM_001305792.1:c.-18-1589_-18-1582del	NM_001305792.1:c.-18-1587_-18-1582del	NM_001305792.1:c.-18-1586_-18-1582del	NM_001305792.1:c.-18-1585_-18-1582del	NM_001305792.1:c.-18-1584_-18-1582del	NM_001305792.1:c.-18-1583_-18-1582del	NM_001305792.1:c.-18-1582del	NM_001305792.1:c.-18-1582dup	NM_001305792.1:c.-18-1584_-18-1582dup	NM_001305792.1:c.-18-1589_-18-1582dup
KIF14 transcript variant 1	NM_014875.2:c.1456-1582=	NM_014875.2:c.1456-1591_1456-1582del	NM_014875.2:c.1456-1589_1456-1582del	NM_014875.2:c.1456-1587_1456-1582del	NM_014875.2:c.1456-1586_1456-1582del	NM_014875.2:c.1456-1585_1456-1582del	NM_014875.2:c.1456-1584_1456-1582del	NM_014875.2:c.1456-1583_1456-1582del	NM_014875.2:c.1456-1582del	NM_014875.2:c.1456-1582dup	NM_014875.2:c.1456-1584_1456-1582dup	NM_014875.2:c.1456-1589_1456-1582dup
KIF14 transcript variant 1	NM_014875.3:c.1456-1582=	NM_014875.3:c.1456-1591_1456-1582del	NM_014875.3:c.1456-1589_1456-1582del	NM_014875.3:c.1456-1587_1456-1582del	NM_014875.3:c.1456-1586_1456-1582del	NM_014875.3:c.1456-1585_1456-1582del	NM_014875.3:c.1456-1584_1456-1582del	NM_014875.3:c.1456-1583_1456-1582del	NM_014875.3:c.1456-1582del	NM_014875.3:c.1456-1582dup	NM_014875.3:c.1456-1584_1456-1582dup	NM_014875.3:c.1456-1589_1456-1582dup
KIF14 transcript variant X1	XM_005245692.1:c.-18-1582=	XM_005245692.1:c.-18-1591_-18-1582del	XM_005245692.1:c.-18-1589_-18-1582del	XM_005245692.1:c.-18-1587_-18-1582del	XM_005245692.1:c.-18-1586_-18-1582del	XM_005245692.1:c.-18-1585_-18-1582del	XM_005245692.1:c.-18-1584_-18-1582del	XM_005245692.1:c.-18-1583_-18-1582del	XM_005245692.1:c.-18-1582del	XM_005245692.1:c.-18-1582dup	XM_005245692.1:c.-18-1584_-18-1582dup	XM_005245692.1:c.-18-1589_-18-1582dup
KIF14 transcript variant X1	XM_011510231.3:c.1456-1582=	XM_011510231.3:c.1456-1591_1456-1582del	XM_011510231.3:c.1456-1589_1456-1582del	XM_011510231.3:c.1456-1587_1456-1582del	XM_011510231.3:c.1456-1586_1456-1582del	XM_011510231.3:c.1456-1585_1456-1582del	XM_011510231.3:c.1456-1584_1456-1582del	XM_011510231.3:c.1456-1583_1456-1582del	XM_011510231.3:c.1456-1582del	XM_011510231.3:c.1456-1582dup	XM_011510231.3:c.1456-1584_1456-1582dup	XM_011510231.3:c.1456-1589_1456-1582dup
KIF14 transcript variant X2	XM_011510232.3:c.1456-1582=	XM_011510232.3:c.1456-1591_1456-1582del	XM_011510232.3:c.1456-1589_1456-1582del	XM_011510232.3:c.1456-1587_1456-1582del	XM_011510232.3:c.1456-1586_1456-1582del	XM_011510232.3:c.1456-1585_1456-1582del	XM_011510232.3:c.1456-1584_1456-1582del	XM_011510232.3:c.1456-1583_1456-1582del	XM_011510232.3:c.1456-1582del	XM_011510232.3:c.1456-1582dup	XM_011510232.3:c.1456-1584_1456-1582dup	XM_011510232.3:c.1456-1589_1456-1582dup
KIF14 transcript variant X3	XM_011510233.3:c.1372-1582=	XM_011510233.3:c.1372-1591_1372-1582del	XM_011510233.3:c.1372-1589_1372-1582del	XM_011510233.3:c.1372-1587_1372-1582del	XM_011510233.3:c.1372-1586_1372-1582del	XM_011510233.3:c.1372-1585_1372-1582del	XM_011510233.3:c.1372-1584_1372-1582del	XM_011510233.3:c.1372-1583_1372-1582del	XM_011510233.3:c.1372-1582del	XM_011510233.3:c.1372-1582dup	XM_011510233.3:c.1372-1584_1372-1582dup	XM_011510233.3:c.1372-1589_1372-1582dup
KIF14 transcript variant X9	XM_011510235.3:c.1084-1582=	XM_011510235.3:c.1084-1591_1084-1582del	XM_011510235.3:c.1084-1589_1084-1582del	XM_011510235.3:c.1084-1587_1084-1582del	XM_011510235.3:c.1084-1586_1084-1582del	XM_011510235.3:c.1084-1585_1084-1582del	XM_011510235.3:c.1084-1584_1084-1582del	XM_011510235.3:c.1084-1583_1084-1582del	XM_011510235.3:c.1084-1582del	XM_011510235.3:c.1084-1582dup	XM_011510235.3:c.1084-1584_1084-1582dup	XM_011510235.3:c.1084-1589_1084-1582dup
KIF14 transcript variant X7	XM_017003006.2:c.1327-1582=	XM_017003006.2:c.1327-1591_1327-1582del	XM_017003006.2:c.1327-1589_1327-1582del	XM_017003006.2:c.1327-1587_1327-1582del	XM_017003006.2:c.1327-1586_1327-1582del	XM_017003006.2:c.1327-1585_1327-1582del	XM_017003006.2:c.1327-1584_1327-1582del	XM_017003006.2:c.1327-1583_1327-1582del	XM_017003006.2:c.1327-1582del	XM_017003006.2:c.1327-1582dup	XM_017003006.2:c.1327-1584_1327-1582dup	XM_017003006.2:c.1327-1589_1327-1582dup
KIF14 transcript variant X13	XM_017003007.2:c.889-1582=	XM_017003007.2:c.889-1591_889-1582del	XM_017003007.2:c.889-1589_889-1582del	XM_017003007.2:c.889-1587_889-1582del	XM_017003007.2:c.889-1586_889-1582del	XM_017003007.2:c.889-1585_889-1582del	XM_017003007.2:c.889-1584_889-1582del	XM_017003007.2:c.889-1583_889-1582del	XM_017003007.2:c.889-1582del	XM_017003007.2:c.889-1582dup	XM_017003007.2:c.889-1584_889-1582dup	XM_017003007.2:c.889-1589_889-1582dup
KIF14 transcript variant X4	XM_047436181.1:c.1372-1582=	XM_047436181.1:c.1372-1591_1372-1582del	XM_047436181.1:c.1372-1589_1372-1582del	XM_047436181.1:c.1372-1587_1372-1582del	XM_047436181.1:c.1372-1586_1372-1582del	XM_047436181.1:c.1372-1585_1372-1582del	XM_047436181.1:c.1372-1584_1372-1582del	XM_047436181.1:c.1372-1583_1372-1582del	XM_047436181.1:c.1372-1582del	XM_047436181.1:c.1372-1582dup	XM_047436181.1:c.1372-1584_1372-1582dup	XM_047436181.1:c.1372-1589_1372-1582dup
KIF14 transcript variant X5	XM_047436184.1:c.1372-1582=	XM_047436184.1:c.1372-1591_1372-1582del	XM_047436184.1:c.1372-1589_1372-1582del	XM_047436184.1:c.1372-1587_1372-1582del	XM_047436184.1:c.1372-1586_1372-1582del	XM_047436184.1:c.1372-1585_1372-1582del	XM_047436184.1:c.1372-1584_1372-1582del	XM_047436184.1:c.1372-1583_1372-1582del	XM_047436184.1:c.1372-1582del	XM_047436184.1:c.1372-1582dup	XM_047436184.1:c.1372-1584_1372-1582dup	XM_047436184.1:c.1372-1589_1372-1582dup
KIF14 transcript variant X6	XM_047436190.1:c.1372-1582=	XM_047436190.1:c.1372-1591_1372-1582del	XM_047436190.1:c.1372-1589_1372-1582del	XM_047436190.1:c.1372-1587_1372-1582del	XM_047436190.1:c.1372-1586_1372-1582del	XM_047436190.1:c.1372-1585_1372-1582del	XM_047436190.1:c.1372-1584_1372-1582del	XM_047436190.1:c.1372-1583_1372-1582del	XM_047436190.1:c.1372-1582del	XM_047436190.1:c.1372-1582dup	XM_047436190.1:c.1372-1584_1372-1582dup	XM_047436190.1:c.1372-1589_1372-1582dup
KIF14 transcript variant X8	XM_047436195.1:c.1243-1582=	XM_047436195.1:c.1243-1591_1243-1582del	XM_047436195.1:c.1243-1589_1243-1582del	XM_047436195.1:c.1243-1587_1243-1582del	XM_047436195.1:c.1243-1586_1243-1582del	XM_047436195.1:c.1243-1585_1243-1582del	XM_047436195.1:c.1243-1584_1243-1582del	XM_047436195.1:c.1243-1583_1243-1582del	XM_047436195.1:c.1243-1582del	XM_047436195.1:c.1243-1582dup	XM_047436195.1:c.1243-1584_1243-1582dup	XM_047436195.1:c.1243-1589_1243-1582dup
KIF14 transcript variant X10	XM_047436197.1:c.1084-1582=	XM_047436197.1:c.1084-1591_1084-1582del	XM_047436197.1:c.1084-1589_1084-1582del	XM_047436197.1:c.1084-1587_1084-1582del	XM_047436197.1:c.1084-1586_1084-1582del	XM_047436197.1:c.1084-1585_1084-1582del	XM_047436197.1:c.1084-1584_1084-1582del	XM_047436197.1:c.1084-1583_1084-1582del	XM_047436197.1:c.1084-1582del	XM_047436197.1:c.1084-1582dup	XM_047436197.1:c.1084-1584_1084-1582dup	XM_047436197.1:c.1084-1589_1084-1582dup
KIF14 transcript variant X11	XM_047436198.1:c.1084-1582=	XM_047436198.1:c.1084-1591_1084-1582del	XM_047436198.1:c.1084-1589_1084-1582del	XM_047436198.1:c.1084-1587_1084-1582del	XM_047436198.1:c.1084-1586_1084-1582del	XM_047436198.1:c.1084-1585_1084-1582del	XM_047436198.1:c.1084-1584_1084-1582del	XM_047436198.1:c.1084-1583_1084-1582del	XM_047436198.1:c.1084-1582del	XM_047436198.1:c.1084-1582dup	XM_047436198.1:c.1084-1584_1084-1582dup	XM_047436198.1:c.1084-1589_1084-1582dup
KIF14 transcript variant X12	XM_047436199.1:c.955-1582=	XM_047436199.1:c.955-1591_955-1582del	XM_047436199.1:c.955-1589_955-1582del	XM_047436199.1:c.955-1587_955-1582del	XM_047436199.1:c.955-1586_955-1582del	XM_047436199.1:c.955-1585_955-1582del	XM_047436199.1:c.955-1584_955-1582del	XM_047436199.1:c.955-1583_955-1582del	XM_047436199.1:c.955-1582del	XM_047436199.1:c.955-1582dup	XM_047436199.1:c.955-1584_955-1582dup	XM_047436199.1:c.955-1589_955-1582dup

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#.

46 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41339243	Mar 15, 2006 (126)
2	HUMANGENOME_JCVI	ss95251843	Feb 13, 2009 (137)
3	HUMANGENOME_JCVI	ss98580615	Mar 15, 2016 (147)
4	PJP	ss294619897	May 09, 2011 (137)
5	PJP	ss294619898	May 09, 2011 (137)
6	BILGI_BIOE	ss666123040	Apr 25, 2013 (138)
7	1000GENOMES	ss1367959198	Aug 21, 2014 (142)
8	EVA_UK10K_ALSPAC	ss1701640402	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1701640561	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709965981	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1709965982	Apr 01, 2015 (144)
12	SWEGEN	ss2988264813	Nov 08, 2017 (151)
13	URBANLAB	ss3646862138	Oct 11, 2018 (152)
14	EVA_DECODE	ss3688406294	Jul 12, 2019 (153)
15	EVA_DECODE	ss3688406295	Jul 12, 2019 (153)
16	EVA_DECODE	ss3688406296	Jul 12, 2019 (153)
17	EVA_DECODE	ss3688406297	Jul 12, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3800203609	Jul 12, 2019 (153)
19	EVA	ss3826586623	Apr 25, 2020 (154)
20	KOGIC	ss3946260296	Apr 25, 2020 (154)
21	KOGIC	ss3946260297	Apr 25, 2020 (154)
22	KOGIC	ss3946260298	Apr 25, 2020 (154)
23	KOGIC	ss3946260299	Apr 25, 2020 (154)
24	GNOMAD	ss4009318223	Apr 25, 2021 (155)
25	GNOMAD	ss4009318224	Apr 25, 2021 (155)
26	GNOMAD	ss4009318226	Apr 25, 2021 (155)
27	GNOMAD	ss4009318227	Apr 25, 2021 (155)
28	GNOMAD	ss4009318228	Apr 25, 2021 (155)
29	GNOMAD	ss4009318229	Apr 25, 2021 (155)
30	GNOMAD	ss4009318230	Apr 25, 2021 (155)
31	GNOMAD	ss4009318231	Apr 25, 2021 (155)
32	TOPMED	ss4479667192	Apr 25, 2021 (155)
33	TOMMO_GENOMICS	ss5147922742	Apr 25, 2021 (155)
34	TOMMO_GENOMICS	ss5147922743	Apr 25, 2021 (155)
35	TOMMO_GENOMICS	ss5147922744	Apr 25, 2021 (155)
36	1000G_HIGH_COVERAGE	ss5245404647	Oct 12, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5245404648	Oct 12, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5245404649	Oct 12, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5245404650	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5245404651	Oct 12, 2022 (156)
41	HUGCELL_USP	ss5445881577	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5445881578	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5445881579	Oct 12, 2022 (156)
44	TOMMO_GENOMICS	ss5675532510	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5675532511	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5675532512	Oct 12, 2022 (156)
47	1000Genomes	NC_000001.10 - 200579638	Oct 11, 2018 (152)
48	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2772620 (NC_000001.10:200579638:A: 3181/3854) Row 2772621 (NC_000001.10:200579637:AAA: 504/3854)	-	Oct 11, 2018 (152)
49	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 2772620 (NC_000001.10:200579638:A: 3181/3854) Row 2772621 (NC_000001.10:200579637:AAA: 504/3854)	-	Oct 11, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 36357348 (NC_000001.11:200610509::A 117/98366) Row 36357349 (NC_000001.11:200610509::AAAAAAAA 1/98394) Row 36357351 (NC_000001.11:200610509:A: 60878/98400)...	-	Apr 25, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 2638297 (NC_000001.11:200610510:AA: 401/1826) Row 2638298 (NC_000001.11:200610511:A: 855/1826) Row 2638299 (NC_000001.11:200610512::A 28/1826)...	-	Apr 25, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 2638297 (NC_000001.11:200610510:AA: 401/1826) Row 2638298 (NC_000001.11:200610511:A: 855/1826) Row 2638299 (NC_000001.11:200610512::A 28/1826)...	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 2638297 (NC_000001.11:200610510:AA: 401/1826) Row 2638298 (NC_000001.11:200610511:A: 855/1826) Row 2638299 (NC_000001.11:200610512::A 28/1826)...	-	Apr 25, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 2638297 (NC_000001.11:200610510:AA: 401/1826) Row 2638298 (NC_000001.11:200610511:A: 855/1826) Row 2638299 (NC_000001.11:200610512::A 28/1826)...	-	Apr 25, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 5892049 (NC_000001.10:200579637:AA: 2640/16712) Row 5892050 (NC_000001.10:200579637:A: 9787/16712) Row 5892051 (NC_000001.10:200579637::A 12/16712)	-	Apr 25, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 5892049 (NC_000001.10:200579637:AA: 2640/16712) Row 5892050 (NC_000001.10:200579637:A: 9787/16712) Row 5892051 (NC_000001.10:200579637::A 12/16712)	-	Apr 25, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 5892049 (NC_000001.10:200579637:AA: 2640/16712) Row 5892050 (NC_000001.10:200579637:A: 9787/16712) Row 5892051 (NC_000001.10:200579637::A 12/16712)	-	Apr 25, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 9369614 (NC_000001.11:200610509:A: 16024/28046) Row 9369615 (NC_000001.11:200610509:AA: 4500/28046) Row 9369616 (NC_000001.11:200610509::A 16/28046)	-	Oct 12, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 9369614 (NC_000001.11:200610509:A: 16024/28046) Row 9369615 (NC_000001.11:200610509:AA: 4500/28046) Row 9369616 (NC_000001.11:200610509::A 16/28046)	-	Oct 12, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 9369614 (NC_000001.11:200610509:A: 16024/28046) Row 9369615 (NC_000001.11:200610509:AA: 4500/28046) Row 9369616 (NC_000001.11:200610509::A 16/28046)	-	Oct 12, 2022 (156)
68	TopMed	NC_000001.11 - 200610510	Apr 25, 2021 (155)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2772620 (NC_000001.10:200579638:A: 3086/3708) Row 2772621 (NC_000001.10:200579637:AAA: 456/3708)	-	Oct 11, 2018 (152)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 2772620 (NC_000001.10:200579638:A: 3086/3708) Row 2772621 (NC_000001.10:200579637:AAA: 456/3708)	-	Oct 11, 2018 (152)
71	ALFA	NC_000001.11 - 200610510	Apr 25, 2021 (155)

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

Associated ID	History Updated (Build)
rs143545676	May 11, 2012 (137)
rs71135372	May 11, 2012 (137)
rs372233678	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5245404651	NC_000001.11:200610509:AAAAAAAAAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4009318231	NC_000001.11:200610509:AAAAAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4009318230	NC_000001.11:200610509:AAAAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3688406297, ss4009318229	NC_000001.11:200610509:AAAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss1701640402, ss1701640561	NC_000001.10:200579637:AAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3946260299, ss4009318228, ss5245404650	NC_000001.11:200610509:AAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3688406296	NC_000001.11:200610510:AAA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss294619897	NC_000001.9:198846260:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss2988264813, ss5147922742	NC_000001.10:200579637:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1709965981, ss1709965982	NC_000001.10:200579638:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4009318227, ss5245404648, ss5445881578, ss5675532511	NC_000001.11:200610509:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3946260296	NC_000001.11:200610510:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3688406295	NC_000001.11:200610511:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss98580615	NT_004487.19:52068298:AA:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss294619898	NC_000001.9:198846280:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
5040862, ss666123040, ss1367959198, ss3826586623, ss5147922743	NC_000001.10:200579637:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
	NC_000001.10:200579638:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3646862138, ss3800203609, ss4009318226, ss5245404647, ss5445881577, ss5675532510	NC_000001.11:200610509:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3946260297	NC_000001.11:200610511:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3688406294	NC_000001.11:200610512:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss41339243	NT_004487.19:52068279:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss98580615	NT_004487.19:52068298:AA:A	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss95251843	NT_004487.19:52068299:A:	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5147922744	NC_000001.10:200579637::A	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4009318223, ss5245404649, ss5445881579, ss5675532512	NC_000001.11:200610509::A	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3946260298	NC_000001.11:200610512::A	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
43273527, ss4479667192	NC_000001.11:200610509::AAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
1732527390	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4009318224	NC_000001.11:200610509::AAAAAAAA	NC_000001.11:200610509:AAAAAAAAAAA… NC_000001.11:200610509:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

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

No publications for rs35647787

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

rs35647787