Name: rs201151434
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.

rs201151434

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:169445866-169445886 (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(CA)₄ / del(CA)₃ / delCACA / de…
del(CA)₄ / del(CA)₃ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄ / dup(CA)₅ / dup(CA)₆ / dup(CA)₇
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.01416 (400/28258, 14KJPN)
dupCA=0.01581 (265/16760, 8.3KJPN)
dupCA=0.00148 (22/14882, ALFA) (+ 2 more)
dupCA=0.0158 (29/1832, Korea1K)
dupCA=0.002 (1/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NEK1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HTRZ	HWEP
Total	Global	14882	ACACACACACACACACACACA=0.99852	ACACACACACACA=0.00000, ACACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00148, ACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACA=0.00000	0.997298	0.002702	0
European	Sub	10813	ACACACACACACACACACACA=0.99797	ACACACACACACA=0.00000, ACACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00203, ACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACACACACACACA=0.00000	0.996199	0.003801	0
African	Sub	2678	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	N/A
African Others	Sub	98	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
African American	Sub	2580	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACACACACA=0.0000	1.0	0.0	N/A
Asian	Sub	106	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	N/A
East Asian	Sub	82	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Other Asian	Sub	24	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Latin American 1	Sub	140	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	N/A
Latin American 2	Sub	592	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	N/A
South Asian	Sub	92	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACACACACA=0.00	1.0	0.0	N/A
Other	Sub	461	ACACACACACACACACACACA=1.000	ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACACACACACACA=0.000	1.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
14KJPN	JAPANESE	Study-wide	28258	- No frequency provided	dupCA=0.01416
8.3KJPN	JAPANESE	Study-wide	16760	- No frequency provided	dupCA=0.01581
Allele Frequency Aggregator	Total	Global	14882	(AC)₁₀A=0.99852	del(CA)₄=0.00000, del(CA)₃=0.00000, delCACA=0.00000, delCA=0.00000, dupCA=0.00148, dupCACA=0.00000, dup(CA)₃=0.00000, dup(CA)₄=0.00000, dup(CA)₅=0.00000, dup(CA)₆=0.00000, dup(CA)₇=0.00000
Allele Frequency Aggregator	European	Sub	10813	(AC)₁₀A=0.99797	del(CA)₄=0.00000, del(CA)₃=0.00000, delCACA=0.00000, delCA=0.00000, dupCA=0.00203, dupCACA=0.00000, dup(CA)₃=0.00000, dup(CA)₄=0.00000, dup(CA)₅=0.00000, dup(CA)₆=0.00000, dup(CA)₇=0.00000
Allele Frequency Aggregator	African	Sub	2678	(AC)₁₀A=1.0000	del(CA)₄=0.0000, del(CA)₃=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)₃=0.0000, dup(CA)₄=0.0000, dup(CA)₅=0.0000, dup(CA)₆=0.0000, dup(CA)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	592	(AC)₁₀A=1.000	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000
Allele Frequency Aggregator	Other	Sub	461	(AC)₁₀A=1.000	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	140	(AC)₁₀A=1.000	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000
Allele Frequency Aggregator	Asian	Sub	106	(AC)₁₀A=1.000	del(CA)₄=0.000, del(CA)₃=0.000, delCACA=0.000, delCA=0.000, dupCA=0.000, dupCACA=0.000, dup(CA)₃=0.000, dup(CA)₄=0.000, dup(CA)₅=0.000, dup(CA)₆=0.000, dup(CA)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(AC)₁₀A=1.00	del(CA)₄=0.00, del(CA)₃=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00, dup(CA)₅=0.00, dup(CA)₆=0.00, dup(CA)₇=0.00
Korean Genome Project	KOREAN	Study-wide	1832	- No frequency provided	dupCA=0.0158
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	dupCA=0.002

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 4	NC_000004.12:g.169445867CA[6]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[7]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[8]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[9]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[11]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[12]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[13]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[14]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[15]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[16]
GRCh38.p14 chr 4	NC_000004.12:g.169445867CA[17]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[6]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[7]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[8]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[9]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[11]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[12]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[13]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[14]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[15]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[16]
GRCh37.p13 chr 4	NC_000004.11:g.170367018CA[17]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[6]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[7]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[8]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[9]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[11]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[12]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[13]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[14]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[15]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[16]
NEK1 RefSeqGene	NG_027982.1:g.171743GT[17]

Gene: NEK1, NIMA related kinase 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NEK1 transcript variant 1	NM_001199397.3:c.2588-762… NM_001199397.3:c.2588-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 3	NM_001199398.3:c.2456-762… NM_001199398.3:c.2456-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 4	NM_001199399.3:c.2297-762… NM_001199399.3:c.2297-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 5	NM_001199400.3:c.2372-762… NM_001199400.3:c.2372-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 6	NM_001374418.1:c.2588-762… NM_001374418.1:c.2588-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 7	NM_001374419.1:c.2504-762… NM_001374419.1:c.2504-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 8	NM_001374420.1:c.2453-762… NM_001374420.1:c.2453-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 9	NM_001374421.1:c.2282-122… NM_001374421.1:c.2282-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant 2	NM_012224.4:c.2504-7626GT… NM_012224.4:c.2504-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant 10	NM_001374422.1:c.	N/A	Genic Downstream Transcript Variant
NEK1 transcript variant 11	NM_001374423.1:c.	N/A	Genic Downstream Transcript Variant
NEK1 transcript variant 12	NR_164630.1:n.	N/A	Intron Variant
NEK1 transcript variant 13	NR_164631.1:n.	N/A	Genic Downstream Transcript Variant
NEK1 transcript variant X3	XM_011532004.2:c.2372-762… XM_011532004.2:c.2372-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant X1	XM_047415731.1:c.2456-762… XM_047415731.1:c.2456-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant X2	XM_047415732.1:c.2588-122… XM_047415732.1:c.2588-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant X4	XM_047415733.1:c.2504-122… XM_047415733.1:c.2504-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant X5	XM_047415734.1:c.2504-122… XM_047415734.1:c.2504-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant X6	XM_047415735.1:c.2456-122… XM_047415735.1:c.2456-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant X7	XM_047415736.1:c.2372-122… XM_047415736.1:c.2372-12220GT[6]	N/A	Intron Variant
NEK1 transcript variant X8	XM_047415737.1:c.1967-762… XM_047415737.1:c.1967-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant X9	XM_047415738.1:c.1967-762… XM_047415738.1:c.1967-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant X10	XM_047415739.1:c.1883-762… XM_047415739.1:c.1883-7626GT[6]	N/A	Intron Variant
NEK1 transcript variant X12	XM_011532005.3:c.	N/A	Genic Downstream Transcript Variant
NEK1 transcript variant X11	XM_047415740.1:c.	N/A	Genic Downstream Transcript Variant
NEK1 transcript variant X13	XM_047415741.1:c.	N/A	Genic Downstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(AC)₁₀A=	del(CA)₄	del(CA)₃	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄	dup(CA)₅	dup(CA)₆	dup(CA)₇
GRCh38.p14 chr 4	NC_000004.12:g.169445866_169445886=	NC_000004.12:g.169445867CA[6]	NC_000004.12:g.169445867CA[7]	NC_000004.12:g.169445867CA[8]	NC_000004.12:g.169445867CA[9]	NC_000004.12:g.169445867CA[11]	NC_000004.12:g.169445867CA[12]	NC_000004.12:g.169445867CA[13]	NC_000004.12:g.169445867CA[14]	NC_000004.12:g.169445867CA[15]	NC_000004.12:g.169445867CA[16]	NC_000004.12:g.169445867CA[17]
GRCh37.p13 chr 4	NC_000004.11:g.170367017_170367037=	NC_000004.11:g.170367018CA[6]	NC_000004.11:g.170367018CA[7]	NC_000004.11:g.170367018CA[8]	NC_000004.11:g.170367018CA[9]	NC_000004.11:g.170367018CA[11]	NC_000004.11:g.170367018CA[12]	NC_000004.11:g.170367018CA[13]	NC_000004.11:g.170367018CA[14]	NC_000004.11:g.170367018CA[15]	NC_000004.11:g.170367018CA[16]	NC_000004.11:g.170367018CA[17]
NEK1 RefSeqGene	NG_027982.1:g.171742_171762=	NG_027982.1:g.171743GT[6]	NG_027982.1:g.171743GT[7]	NG_027982.1:g.171743GT[8]	NG_027982.1:g.171743GT[9]	NG_027982.1:g.171743GT[11]	NG_027982.1:g.171743GT[12]	NG_027982.1:g.171743GT[13]	NG_027982.1:g.171743GT[14]	NG_027982.1:g.171743GT[15]	NG_027982.1:g.171743GT[16]	NG_027982.1:g.171743GT[17]
NEK1 transcript variant 1	NM_001199397.1:c.2588-7607=	NM_001199397.1:c.2588-7626GT[6]	NM_001199397.1:c.2588-7626GT[7]	NM_001199397.1:c.2588-7626GT[8]	NM_001199397.1:c.2588-7626GT[9]	NM_001199397.1:c.2588-7626GT[11]	NM_001199397.1:c.2588-7626GT[12]	NM_001199397.1:c.2588-7626GT[13]	NM_001199397.1:c.2588-7626GT[14]	NM_001199397.1:c.2588-7626GT[15]	NM_001199397.1:c.2588-7626GT[16]	NM_001199397.1:c.2588-7626GT[17]
NEK1 transcript variant 1	NM_001199397.3:c.2588-7607=	NM_001199397.3:c.2588-7626GT[6]	NM_001199397.3:c.2588-7626GT[7]	NM_001199397.3:c.2588-7626GT[8]	NM_001199397.3:c.2588-7626GT[9]	NM_001199397.3:c.2588-7626GT[11]	NM_001199397.3:c.2588-7626GT[12]	NM_001199397.3:c.2588-7626GT[13]	NM_001199397.3:c.2588-7626GT[14]	NM_001199397.3:c.2588-7626GT[15]	NM_001199397.3:c.2588-7626GT[16]	NM_001199397.3:c.2588-7626GT[17]
NEK1 transcript variant 3	NM_001199398.1:c.2456-7607=	NM_001199398.1:c.2456-7626GT[6]	NM_001199398.1:c.2456-7626GT[7]	NM_001199398.1:c.2456-7626GT[8]	NM_001199398.1:c.2456-7626GT[9]	NM_001199398.1:c.2456-7626GT[11]	NM_001199398.1:c.2456-7626GT[12]	NM_001199398.1:c.2456-7626GT[13]	NM_001199398.1:c.2456-7626GT[14]	NM_001199398.1:c.2456-7626GT[15]	NM_001199398.1:c.2456-7626GT[16]	NM_001199398.1:c.2456-7626GT[17]
NEK1 transcript variant 3	NM_001199398.3:c.2456-7607=	NM_001199398.3:c.2456-7626GT[6]	NM_001199398.3:c.2456-7626GT[7]	NM_001199398.3:c.2456-7626GT[8]	NM_001199398.3:c.2456-7626GT[9]	NM_001199398.3:c.2456-7626GT[11]	NM_001199398.3:c.2456-7626GT[12]	NM_001199398.3:c.2456-7626GT[13]	NM_001199398.3:c.2456-7626GT[14]	NM_001199398.3:c.2456-7626GT[15]	NM_001199398.3:c.2456-7626GT[16]	NM_001199398.3:c.2456-7626GT[17]
NEK1 transcript variant 4	NM_001199399.1:c.2297-7607=	NM_001199399.1:c.2297-7626GT[6]	NM_001199399.1:c.2297-7626GT[7]	NM_001199399.1:c.2297-7626GT[8]	NM_001199399.1:c.2297-7626GT[9]	NM_001199399.1:c.2297-7626GT[11]	NM_001199399.1:c.2297-7626GT[12]	NM_001199399.1:c.2297-7626GT[13]	NM_001199399.1:c.2297-7626GT[14]	NM_001199399.1:c.2297-7626GT[15]	NM_001199399.1:c.2297-7626GT[16]	NM_001199399.1:c.2297-7626GT[17]
NEK1 transcript variant 4	NM_001199399.3:c.2297-7607=	NM_001199399.3:c.2297-7626GT[6]	NM_001199399.3:c.2297-7626GT[7]	NM_001199399.3:c.2297-7626GT[8]	NM_001199399.3:c.2297-7626GT[9]	NM_001199399.3:c.2297-7626GT[11]	NM_001199399.3:c.2297-7626GT[12]	NM_001199399.3:c.2297-7626GT[13]	NM_001199399.3:c.2297-7626GT[14]	NM_001199399.3:c.2297-7626GT[15]	NM_001199399.3:c.2297-7626GT[16]	NM_001199399.3:c.2297-7626GT[17]
NEK1 transcript variant 5	NM_001199400.1:c.2372-7607=	NM_001199400.1:c.2372-7626GT[6]	NM_001199400.1:c.2372-7626GT[7]	NM_001199400.1:c.2372-7626GT[8]	NM_001199400.1:c.2372-7626GT[9]	NM_001199400.1:c.2372-7626GT[11]	NM_001199400.1:c.2372-7626GT[12]	NM_001199400.1:c.2372-7626GT[13]	NM_001199400.1:c.2372-7626GT[14]	NM_001199400.1:c.2372-7626GT[15]	NM_001199400.1:c.2372-7626GT[16]	NM_001199400.1:c.2372-7626GT[17]
NEK1 transcript variant 5	NM_001199400.3:c.2372-7607=	NM_001199400.3:c.2372-7626GT[6]	NM_001199400.3:c.2372-7626GT[7]	NM_001199400.3:c.2372-7626GT[8]	NM_001199400.3:c.2372-7626GT[9]	NM_001199400.3:c.2372-7626GT[11]	NM_001199400.3:c.2372-7626GT[12]	NM_001199400.3:c.2372-7626GT[13]	NM_001199400.3:c.2372-7626GT[14]	NM_001199400.3:c.2372-7626GT[15]	NM_001199400.3:c.2372-7626GT[16]	NM_001199400.3:c.2372-7626GT[17]
NEK1 transcript variant 6	NM_001374418.1:c.2588-7607=	NM_001374418.1:c.2588-7626GT[6]	NM_001374418.1:c.2588-7626GT[7]	NM_001374418.1:c.2588-7626GT[8]	NM_001374418.1:c.2588-7626GT[9]	NM_001374418.1:c.2588-7626GT[11]	NM_001374418.1:c.2588-7626GT[12]	NM_001374418.1:c.2588-7626GT[13]	NM_001374418.1:c.2588-7626GT[14]	NM_001374418.1:c.2588-7626GT[15]	NM_001374418.1:c.2588-7626GT[16]	NM_001374418.1:c.2588-7626GT[17]
NEK1 transcript variant 7	NM_001374419.1:c.2504-7607=	NM_001374419.1:c.2504-7626GT[6]	NM_001374419.1:c.2504-7626GT[7]	NM_001374419.1:c.2504-7626GT[8]	NM_001374419.1:c.2504-7626GT[9]	NM_001374419.1:c.2504-7626GT[11]	NM_001374419.1:c.2504-7626GT[12]	NM_001374419.1:c.2504-7626GT[13]	NM_001374419.1:c.2504-7626GT[14]	NM_001374419.1:c.2504-7626GT[15]	NM_001374419.1:c.2504-7626GT[16]	NM_001374419.1:c.2504-7626GT[17]
NEK1 transcript variant 8	NM_001374420.1:c.2453-7607=	NM_001374420.1:c.2453-7626GT[6]	NM_001374420.1:c.2453-7626GT[7]	NM_001374420.1:c.2453-7626GT[8]	NM_001374420.1:c.2453-7626GT[9]	NM_001374420.1:c.2453-7626GT[11]	NM_001374420.1:c.2453-7626GT[12]	NM_001374420.1:c.2453-7626GT[13]	NM_001374420.1:c.2453-7626GT[14]	NM_001374420.1:c.2453-7626GT[15]	NM_001374420.1:c.2453-7626GT[16]	NM_001374420.1:c.2453-7626GT[17]
NEK1 transcript variant 9	NM_001374421.1:c.2282-12201=	NM_001374421.1:c.2282-12220GT[6]	NM_001374421.1:c.2282-12220GT[7]	NM_001374421.1:c.2282-12220GT[8]	NM_001374421.1:c.2282-12220GT[9]	NM_001374421.1:c.2282-12220GT[11]	NM_001374421.1:c.2282-12220GT[12]	NM_001374421.1:c.2282-12220GT[13]	NM_001374421.1:c.2282-12220GT[14]	NM_001374421.1:c.2282-12220GT[15]	NM_001374421.1:c.2282-12220GT[16]	NM_001374421.1:c.2282-12220GT[17]
NEK1 transcript variant 2	NM_012224.2:c.2504-7607=	NM_012224.2:c.2504-7626GT[6]	NM_012224.2:c.2504-7626GT[7]	NM_012224.2:c.2504-7626GT[8]	NM_012224.2:c.2504-7626GT[9]	NM_012224.2:c.2504-7626GT[11]	NM_012224.2:c.2504-7626GT[12]	NM_012224.2:c.2504-7626GT[13]	NM_012224.2:c.2504-7626GT[14]	NM_012224.2:c.2504-7626GT[15]	NM_012224.2:c.2504-7626GT[16]	NM_012224.2:c.2504-7626GT[17]
NEK1 transcript variant 2	NM_012224.4:c.2504-7607=	NM_012224.4:c.2504-7626GT[6]	NM_012224.4:c.2504-7626GT[7]	NM_012224.4:c.2504-7626GT[8]	NM_012224.4:c.2504-7626GT[9]	NM_012224.4:c.2504-7626GT[11]	NM_012224.4:c.2504-7626GT[12]	NM_012224.4:c.2504-7626GT[13]	NM_012224.4:c.2504-7626GT[14]	NM_012224.4:c.2504-7626GT[15]	NM_012224.4:c.2504-7626GT[16]	NM_012224.4:c.2504-7626GT[17]
NEK1 transcript variant X1	XM_005263027.1:c.2504-7607=	XM_005263027.1:c.2504-7626GT[6]	XM_005263027.1:c.2504-7626GT[7]	XM_005263027.1:c.2504-7626GT[8]	XM_005263027.1:c.2504-7626GT[9]	XM_005263027.1:c.2504-7626GT[11]	XM_005263027.1:c.2504-7626GT[12]	XM_005263027.1:c.2504-7626GT[13]	XM_005263027.1:c.2504-7626GT[14]	XM_005263027.1:c.2504-7626GT[15]	XM_005263027.1:c.2504-7626GT[16]	XM_005263027.1:c.2504-7626GT[17]
NEK1 transcript variant X2	XM_005263028.1:c.2372-7607=	XM_005263028.1:c.2372-7626GT[6]	XM_005263028.1:c.2372-7626GT[7]	XM_005263028.1:c.2372-7626GT[8]	XM_005263028.1:c.2372-7626GT[9]	XM_005263028.1:c.2372-7626GT[11]	XM_005263028.1:c.2372-7626GT[12]	XM_005263028.1:c.2372-7626GT[13]	XM_005263028.1:c.2372-7626GT[14]	XM_005263028.1:c.2372-7626GT[15]	XM_005263028.1:c.2372-7626GT[16]	XM_005263028.1:c.2372-7626GT[17]
NEK1 transcript variant X3	XM_011532004.2:c.2372-7607=	XM_011532004.2:c.2372-7626GT[6]	XM_011532004.2:c.2372-7626GT[7]	XM_011532004.2:c.2372-7626GT[8]	XM_011532004.2:c.2372-7626GT[9]	XM_011532004.2:c.2372-7626GT[11]	XM_011532004.2:c.2372-7626GT[12]	XM_011532004.2:c.2372-7626GT[13]	XM_011532004.2:c.2372-7626GT[14]	XM_011532004.2:c.2372-7626GT[15]	XM_011532004.2:c.2372-7626GT[16]	XM_011532004.2:c.2372-7626GT[17]
NEK1 transcript variant X1	XM_047415731.1:c.2456-7607=	XM_047415731.1:c.2456-7626GT[6]	XM_047415731.1:c.2456-7626GT[7]	XM_047415731.1:c.2456-7626GT[8]	XM_047415731.1:c.2456-7626GT[9]	XM_047415731.1:c.2456-7626GT[11]	XM_047415731.1:c.2456-7626GT[12]	XM_047415731.1:c.2456-7626GT[13]	XM_047415731.1:c.2456-7626GT[14]	XM_047415731.1:c.2456-7626GT[15]	XM_047415731.1:c.2456-7626GT[16]	XM_047415731.1:c.2456-7626GT[17]
NEK1 transcript variant X2	XM_047415732.1:c.2588-12201=	XM_047415732.1:c.2588-12220GT[6]	XM_047415732.1:c.2588-12220GT[7]	XM_047415732.1:c.2588-12220GT[8]	XM_047415732.1:c.2588-12220GT[9]	XM_047415732.1:c.2588-12220GT[11]	XM_047415732.1:c.2588-12220GT[12]	XM_047415732.1:c.2588-12220GT[13]	XM_047415732.1:c.2588-12220GT[14]	XM_047415732.1:c.2588-12220GT[15]	XM_047415732.1:c.2588-12220GT[16]	XM_047415732.1:c.2588-12220GT[17]
NEK1 transcript variant X4	XM_047415733.1:c.2504-12201=	XM_047415733.1:c.2504-12220GT[6]	XM_047415733.1:c.2504-12220GT[7]	XM_047415733.1:c.2504-12220GT[8]	XM_047415733.1:c.2504-12220GT[9]	XM_047415733.1:c.2504-12220GT[11]	XM_047415733.1:c.2504-12220GT[12]	XM_047415733.1:c.2504-12220GT[13]	XM_047415733.1:c.2504-12220GT[14]	XM_047415733.1:c.2504-12220GT[15]	XM_047415733.1:c.2504-12220GT[16]	XM_047415733.1:c.2504-12220GT[17]
NEK1 transcript variant X5	XM_047415734.1:c.2504-12201=	XM_047415734.1:c.2504-12220GT[6]	XM_047415734.1:c.2504-12220GT[7]	XM_047415734.1:c.2504-12220GT[8]	XM_047415734.1:c.2504-12220GT[9]	XM_047415734.1:c.2504-12220GT[11]	XM_047415734.1:c.2504-12220GT[12]	XM_047415734.1:c.2504-12220GT[13]	XM_047415734.1:c.2504-12220GT[14]	XM_047415734.1:c.2504-12220GT[15]	XM_047415734.1:c.2504-12220GT[16]	XM_047415734.1:c.2504-12220GT[17]
NEK1 transcript variant X6	XM_047415735.1:c.2456-12201=	XM_047415735.1:c.2456-12220GT[6]	XM_047415735.1:c.2456-12220GT[7]	XM_047415735.1:c.2456-12220GT[8]	XM_047415735.1:c.2456-12220GT[9]	XM_047415735.1:c.2456-12220GT[11]	XM_047415735.1:c.2456-12220GT[12]	XM_047415735.1:c.2456-12220GT[13]	XM_047415735.1:c.2456-12220GT[14]	XM_047415735.1:c.2456-12220GT[15]	XM_047415735.1:c.2456-12220GT[16]	XM_047415735.1:c.2456-12220GT[17]
NEK1 transcript variant X7	XM_047415736.1:c.2372-12201=	XM_047415736.1:c.2372-12220GT[6]	XM_047415736.1:c.2372-12220GT[7]	XM_047415736.1:c.2372-12220GT[8]	XM_047415736.1:c.2372-12220GT[9]	XM_047415736.1:c.2372-12220GT[11]	XM_047415736.1:c.2372-12220GT[12]	XM_047415736.1:c.2372-12220GT[13]	XM_047415736.1:c.2372-12220GT[14]	XM_047415736.1:c.2372-12220GT[15]	XM_047415736.1:c.2372-12220GT[16]	XM_047415736.1:c.2372-12220GT[17]
NEK1 transcript variant X8	XM_047415737.1:c.1967-7607=	XM_047415737.1:c.1967-7626GT[6]	XM_047415737.1:c.1967-7626GT[7]	XM_047415737.1:c.1967-7626GT[8]	XM_047415737.1:c.1967-7626GT[9]	XM_047415737.1:c.1967-7626GT[11]	XM_047415737.1:c.1967-7626GT[12]	XM_047415737.1:c.1967-7626GT[13]	XM_047415737.1:c.1967-7626GT[14]	XM_047415737.1:c.1967-7626GT[15]	XM_047415737.1:c.1967-7626GT[16]	XM_047415737.1:c.1967-7626GT[17]
NEK1 transcript variant X9	XM_047415738.1:c.1967-7607=	XM_047415738.1:c.1967-7626GT[6]	XM_047415738.1:c.1967-7626GT[7]	XM_047415738.1:c.1967-7626GT[8]	XM_047415738.1:c.1967-7626GT[9]	XM_047415738.1:c.1967-7626GT[11]	XM_047415738.1:c.1967-7626GT[12]	XM_047415738.1:c.1967-7626GT[13]	XM_047415738.1:c.1967-7626GT[14]	XM_047415738.1:c.1967-7626GT[15]	XM_047415738.1:c.1967-7626GT[16]	XM_047415738.1:c.1967-7626GT[17]
NEK1 transcript variant X10	XM_047415739.1:c.1883-7607=	XM_047415739.1:c.1883-7626GT[6]	XM_047415739.1:c.1883-7626GT[7]	XM_047415739.1:c.1883-7626GT[8]	XM_047415739.1:c.1883-7626GT[9]	XM_047415739.1:c.1883-7626GT[11]	XM_047415739.1:c.1883-7626GT[12]	XM_047415739.1:c.1883-7626GT[13]	XM_047415739.1:c.1883-7626GT[14]	XM_047415739.1:c.1883-7626GT[15]	XM_047415739.1:c.1883-7626GT[16]	XM_047415739.1:c.1883-7626GT[17]

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#.

17 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GMI	ss288596408	May 04, 2012 (137)
2	MCHAISSO	ss3065003254	Nov 08, 2017 (151)
3	ACPOP	ss3731854447	Jul 13, 2019 (153)
4	KOGIC	ss3955641483	Apr 26, 2020 (154)
5	GNOMAD	ss4125275879	Apr 26, 2021 (155)
6	GNOMAD	ss4125275880	Apr 26, 2021 (155)
7	GNOMAD	ss4125275881	Apr 26, 2021 (155)
8	GNOMAD	ss4125275882	Apr 26, 2021 (155)
9	GNOMAD	ss4125275883	Apr 26, 2021 (155)
10	GNOMAD	ss4125275884	Apr 26, 2021 (155)
11	GNOMAD	ss4125275885	Apr 26, 2021 (155)
12	GNOMAD	ss4125275937	Apr 26, 2021 (155)
13	GNOMAD	ss4125275938	Apr 26, 2021 (155)
14	GNOMAD	ss4125275939	Apr 26, 2021 (155)
15	GNOMAD	ss4125275940	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5169265013	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5704604021	Oct 17, 2022 (156)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108253 (NC_000004.12:169445865::AC 897/131540) Row 173108254 (NC_000004.12:169445865::ACAC 58/131578) Row 173108255 (NC_000004.12:169445865::ACACAC 0/131576)...	-	Apr 26, 2021 (155)
29	Korean Genome Project	NC_000004.12 - 169445866	Apr 26, 2020 (154)
30	Northern Sweden	NC_000004.11 - 170367017	Jul 13, 2019 (153)
31	8.3KJPN	NC_000004.11 - 170367017	Apr 26, 2021 (155)
32	14KJPN	NC_000004.12 - 169445866	Oct 17, 2022 (156)
33	ALFA	NC_000004.12 - 169445866	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)
rs935878232	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4125275940	NC_000004.12:169445865:ACACACAC:	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACA	(self)
ss4125275939	NC_000004.12:169445865:ACACAC:	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACA	(self)
ss4125275938	NC_000004.12:169445865:ACAC:	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACA	(self)
ss4125275937	NC_000004.12:169445865:AC:	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss288596408	NC_000004.10:170603612::CA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
5139312, 27234320, ss3731854447, ss5169265013	NC_000004.11:170367016::AC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
12019484, 38441125, ss3955641483, ss4125275879, ss5704604021	NC_000004.12:169445865::AC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3065003254, ss4125275880	NC_000004.12:169445865::ACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4125275881	NC_000004.12:169445865::ACACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss4125275882	NC_000004.12:169445865::ACACACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
ss4125275883	NC_000004.12:169445865::ACACACACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACA	(self)
ss4125275884	NC_000004.12:169445865::ACACACACAC… NC_000004.12:169445865::ACACACACACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA	(self)
ss4125275885	NC_000004.12:169445865::ACACACACAC… NC_000004.12:169445865::ACACACACACACAC	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(self)
8622689085	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	NC_000004.12:169445865:ACACACACACA… NC_000004.12:169445865:ACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA	(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 rs201151434

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs201151434