Name: rs70964204
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.

rs70964204

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:169445850-169445866 (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(TA)₃ / delTATA / delTA / dupTA…
del(TA)₃ / delTATA / delTA / dupTA / dupTATA / dup(TA)₃ / dup(TA)₄ / dup(TA)₅ / ins(TA)₅C(AT)₁₇A / dup(TA)₆ / dup(TA)₇ / dup(TA)₈ / ins(TA)₉ / ins(TA)₁₀ / ins(TA)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: dupTA=0.2924 (2137/7308, ALFA)
dupTA=0.35 (14/40, GENOME_DK)

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	Alt HMOZ	HTRZ	HWEP
Total	Global	7308	ATATATATATATATATA=0.6723	ATATATATATATA=0.0000, ATATATATATATATA=0.0001, ATATATATATATATATATA=0.2924, ATATATATATATATATATATA=0.0348, ATATATATATA=0.0001, ATATATATATATATATATATATATA=0.0001, ATATATATATATATATATATATATATATA=0.0001, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATATATA=0.0000	0.552485	0.14731	0.300206	32
European	Sub	6446	ATATATATATATATATA=0.6292	ATATATATATATA=0.0000, ATATATATATATATA=0.0002, ATATATATATATATATATA=0.3307, ATATATATATATATATATATA=0.0394, ATATATATATA=0.0002, ATATATATATATATATATATATATA=0.0002, ATATATATATATATATATATATATATATA=0.0002, ATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATATA=0.0000, ATATATATATATATATATATATATATATATATATATATA=0.0000	0.488552	0.168013	0.343434	32
African	Sub	582	ATATATATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATATA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
African American	Sub	564	ATATATATATATATATA=1.000	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATATA=0.000, ATATATATATATATATATATA=0.000, ATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATATA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	ATATATATATATATATA=1.0	ATATATATATATA=0.0, ATATATATATATATA=0.0, ATATATATATATATATATA=0.0, ATATATATATATATATATATA=0.0, ATATATATATA=0.0, ATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATATATA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	ATATATATATATATATA=1.0	ATATATATATATA=0.0, ATATATATATATATA=0.0, ATATATATATATATATATA=0.0, ATATATATATATATATATATA=0.0, ATATATATATA=0.0, ATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATATA=0.0, ATATATATATATATATATATATATATATATATATATATA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	ATATATATATATATATA=0	ATATATATATATA=0, ATATATATATATATA=0, ATATATATATATATATATA=0, ATATATATATATATATATATA=0, ATATATATATA=0, ATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATA=0, ATATATATATATATATATATATA=0, ATATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATATATATATA=0, ATATATATATATATATATATATATATATATATATATATA=0	0	0	0	N/A
Latin American 1	Sub	42	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	94	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	38	ATATATATATATATATA=1.00	ATATATATATATA=0.00, ATATATATATATATA=0.00, ATATATATATATATATATA=0.00, ATATATATATATATATATATA=0.00, ATATATATATA=0.00, ATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATA=0.00, ATATATATATATATATATATATATATATATATATATATA=0.00	1.0	0.0	0.0	N/A
Other	Sub	102	ATATATATATATATATA=0.951	ATATATATATATA=0.000, ATATATATATATATA=0.000, ATATATATATATATATATA=0.049, ATATATATATATATATATATA=0.000, ATATATATATA=0.000, ATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATA=0.000, ATATATATATATATATATATATATATATATATATATATA=0.000	0.941176	0.039216	0.019608	17

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7308	(AT)₈A=0.6723	del(TA)₃=0.0001, delTATA=0.0000, delTA=0.0001, dupTA=0.2924, dupTATA=0.0348, dup(TA)₃=0.0000, dup(TA)₄=0.0001, dup(TA)₅=0.0000, dup(TA)₆=0.0001, dup(TA)₇=0.0000, dup(TA)₈=0.0000, ins(TA)₉=0.0000, ins(TA)₁₀=0.0000, ins(TA)₁₁=0.0000
Allele Frequency Aggregator	European	Sub	6446	(AT)₈A=0.6292	del(TA)₃=0.0002, delTATA=0.0000, delTA=0.0002, dupTA=0.3307, dupTATA=0.0394, dup(TA)₃=0.0000, dup(TA)₄=0.0002, dup(TA)₅=0.0000, dup(TA)₆=0.0002, dup(TA)₇=0.0000, dup(TA)₈=0.0000, ins(TA)₉=0.0000, ins(TA)₁₀=0.0000, ins(TA)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	582	(AT)₈A=1.000	del(TA)₃=0.000, delTATA=0.000, delTA=0.000, dupTA=0.000, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000, dup(TA)₇=0.000, dup(TA)₈=0.000, ins(TA)₉=0.000, ins(TA)₁₀=0.000, ins(TA)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	102	(AT)₈A=0.951	del(TA)₃=0.000, delTATA=0.000, delTA=0.000, dupTA=0.049, dupTATA=0.000, dup(TA)₃=0.000, dup(TA)₄=0.000, dup(TA)₅=0.000, dup(TA)₆=0.000, dup(TA)₇=0.000, dup(TA)₈=0.000, ins(TA)₉=0.000, ins(TA)₁₀=0.000, ins(TA)₁₁=0.000
Allele Frequency Aggregator	Latin American 2	Sub	94	(AT)₈A=1.00	del(TA)₃=0.00, delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00, dup(TA)₇=0.00, dup(TA)₈=0.00, ins(TA)₉=0.00, ins(TA)₁₀=0.00, ins(TA)₁₁=0.00
Allele Frequency Aggregator	Latin American 1	Sub	42	(AT)₈A=1.00	del(TA)₃=0.00, delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00, dup(TA)₇=0.00, dup(TA)₈=0.00, ins(TA)₉=0.00, ins(TA)₁₀=0.00, ins(TA)₁₁=0.00
Allele Frequency Aggregator	South Asian	Sub	38	(AT)₈A=1.00	del(TA)₃=0.00, delTATA=0.00, delTA=0.00, dupTA=0.00, dupTATA=0.00, dup(TA)₃=0.00, dup(TA)₄=0.00, dup(TA)₅=0.00, dup(TA)₆=0.00, dup(TA)₇=0.00, dup(TA)₈=0.00, ins(TA)₉=0.00, ins(TA)₁₀=0.00, ins(TA)₁₁=0.00
Allele Frequency Aggregator	Asian	Sub	4	(AT)₈A=1.0	del(TA)₃=0.0, delTATA=0.0, delTA=0.0, dupTA=0.0, dupTATA=0.0, dup(TA)₃=0.0, dup(TA)₄=0.0, dup(TA)₅=0.0, dup(TA)₆=0.0, dup(TA)₇=0.0, dup(TA)₈=0.0, ins(TA)₉=0.0, ins(TA)₁₀=0.0, ins(TA)₁₁=0.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupTA=0.35

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.169445851TA[5]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[6]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[7]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[9]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[10]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[11]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[12]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[13]
GRCh38.p14 chr 4	NC_000004.12:g.169445850_169445866AT[13]ACATATATATATATATATATATATATATATATATATA[1]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[14]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[15]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[16]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[17]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[18]
GRCh38.p14 chr 4	NC_000004.12:g.169445851TA[19]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[5]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[6]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[7]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[9]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[10]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[11]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[12]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[13]
GRCh37.p13 chr 4	NC_000004.11:g.170367001_170367017AT[13]ACATATATATATATATATATATATATATATATATATA[1]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[14]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[15]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[16]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[17]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[18]
GRCh37.p13 chr 4	NC_000004.11:g.170367002TA[19]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[5]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[6]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[7]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[9]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[10]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[11]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[12]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[13]
NEK1 RefSeqGene	NG_027982.1:g.171762_171778TA[17]TGTATATATATATATATATATATATATAT[1]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[14]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[15]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[16]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[17]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[18]
NEK1 RefSeqGene	NG_027982.1:g.171763AT[19]

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

Molecule type	Change	Amino acid[Codon]	SO Term
NEK1 transcript variant 1	NM_001199397.3:c.2588-760… NM_001199397.3:c.2588-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 3	NM_001199398.3:c.2456-760… NM_001199398.3:c.2456-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 4	NM_001199399.3:c.2297-760… NM_001199399.3:c.2297-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 5	NM_001199400.3:c.2372-760… NM_001199400.3:c.2372-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 6	NM_001374418.1:c.2588-760… NM_001374418.1:c.2588-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 7	NM_001374419.1:c.2504-760… NM_001374419.1:c.2504-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 8	NM_001374420.1:c.2453-760… NM_001374420.1:c.2453-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant 9	NM_001374421.1:c.2282-122… NM_001374421.1:c.2282-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant 2	NM_012224.4:c.2504-7606AT… NM_012224.4:c.2504-7606AT[5]	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.2372-760… XM_011532004.2:c.2372-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant X1	XM_047415731.1:c.2456-760… XM_047415731.1:c.2456-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant X2	XM_047415732.1:c.2588-122… XM_047415732.1:c.2588-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant X4	XM_047415733.1:c.2504-122… XM_047415733.1:c.2504-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant X5	XM_047415734.1:c.2504-122… XM_047415734.1:c.2504-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant X6	XM_047415735.1:c.2456-122… XM_047415735.1:c.2456-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant X7	XM_047415736.1:c.2372-122… XM_047415736.1:c.2372-12200AT[5]	N/A	Intron Variant
NEK1 transcript variant X8	XM_047415737.1:c.1967-760… XM_047415737.1:c.1967-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant X9	XM_047415738.1:c.1967-760… XM_047415738.1:c.1967-7606AT[5]	N/A	Intron Variant
NEK1 transcript variant X10	XM_047415739.1:c.1883-760… XM_047415739.1:c.1883-7606AT[5]	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	(AT)₈A=	del(TA)₃	delTATA	delTA	dupTA	dupTATA	dup(TA)₃	dup(TA)₄	dup(TA)₅	ins(TA)₅C(AT)₁₇A	dup(TA)₆	dup(TA)₇	dup(TA)₈	ins(TA)₉	ins(TA)₁₀	ins(TA)₁₁
GRCh38.p14 chr 4	NC_000004.12:g.169445850_169445866=	NC_000004.12:g.169445851TA[5]	NC_000004.12:g.169445851TA[6]	NC_000004.12:g.169445851TA[7]	NC_000004.12:g.169445851TA[9]	NC_000004.12:g.169445851TA[10]	NC_000004.12:g.169445851TA[11]	NC_000004.12:g.169445851TA[12]	NC_000004.12:g.169445851TA[13]	NC_000004.12:g.169445850_169445866AT[13]ACATATATATATATATATATATATATATATATATATA[1]	NC_000004.12:g.169445851TA[14]	NC_000004.12:g.169445851TA[15]	NC_000004.12:g.169445851TA[16]	NC_000004.12:g.169445851TA[17]	NC_000004.12:g.169445851TA[18]	NC_000004.12:g.169445851TA[19]
GRCh37.p13 chr 4	NC_000004.11:g.170367001_170367017=	NC_000004.11:g.170367002TA[5]	NC_000004.11:g.170367002TA[6]	NC_000004.11:g.170367002TA[7]	NC_000004.11:g.170367002TA[9]	NC_000004.11:g.170367002TA[10]	NC_000004.11:g.170367002TA[11]	NC_000004.11:g.170367002TA[12]	NC_000004.11:g.170367002TA[13]	NC_000004.11:g.170367001_170367017AT[13]ACATATATATATATATATATATATATATATATATATA[1]	NC_000004.11:g.170367002TA[14]	NC_000004.11:g.170367002TA[15]	NC_000004.11:g.170367002TA[16]	NC_000004.11:g.170367002TA[17]	NC_000004.11:g.170367002TA[18]	NC_000004.11:g.170367002TA[19]
NEK1 RefSeqGene	NG_027982.1:g.171762_171778=	NG_027982.1:g.171763AT[5]	NG_027982.1:g.171763AT[6]	NG_027982.1:g.171763AT[7]	NG_027982.1:g.171763AT[9]	NG_027982.1:g.171763AT[10]	NG_027982.1:g.171763AT[11]	NG_027982.1:g.171763AT[12]	NG_027982.1:g.171763AT[13]	NG_027982.1:g.171762_171778TA[17]TGTATATATATATATATATATATATATAT[1]	NG_027982.1:g.171763AT[14]	NG_027982.1:g.171763AT[15]	NG_027982.1:g.171763AT[16]	NG_027982.1:g.171763AT[17]	NG_027982.1:g.171763AT[18]	NG_027982.1:g.171763AT[19]
NEK1 transcript variant 1	NM_001199397.1:c.2588-7591=	NM_001199397.1:c.2588-7606AT[5]	NM_001199397.1:c.2588-7606AT[6]	NM_001199397.1:c.2588-7606AT[7]	NM_001199397.1:c.2588-7606AT[9]	NM_001199397.1:c.2588-7606AT[10]	NM_001199397.1:c.2588-7606AT[11]	NM_001199397.1:c.2588-7606AT[12]	NM_001199397.1:c.2588-7606AT[13]	NM_001199397.1:c.2588-7591_2588-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199397.1:c.2588-7606AT[14]	NM_001199397.1:c.2588-7606AT[15]	NM_001199397.1:c.2588-7606AT[16]	NM_001199397.1:c.2588-7606AT[17]	NM_001199397.1:c.2588-7606AT[18]	NM_001199397.1:c.2588-7606AT[19]
NEK1 transcript variant 1	NM_001199397.3:c.2588-7591=	NM_001199397.3:c.2588-7606AT[5]	NM_001199397.3:c.2588-7606AT[6]	NM_001199397.3:c.2588-7606AT[7]	NM_001199397.3:c.2588-7606AT[9]	NM_001199397.3:c.2588-7606AT[10]	NM_001199397.3:c.2588-7606AT[11]	NM_001199397.3:c.2588-7606AT[12]	NM_001199397.3:c.2588-7606AT[13]	NM_001199397.3:c.2588-7591_2588-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199397.3:c.2588-7606AT[14]	NM_001199397.3:c.2588-7606AT[15]	NM_001199397.3:c.2588-7606AT[16]	NM_001199397.3:c.2588-7606AT[17]	NM_001199397.3:c.2588-7606AT[18]	NM_001199397.3:c.2588-7606AT[19]
NEK1 transcript variant 3	NM_001199398.1:c.2456-7591=	NM_001199398.1:c.2456-7606AT[5]	NM_001199398.1:c.2456-7606AT[6]	NM_001199398.1:c.2456-7606AT[7]	NM_001199398.1:c.2456-7606AT[9]	NM_001199398.1:c.2456-7606AT[10]	NM_001199398.1:c.2456-7606AT[11]	NM_001199398.1:c.2456-7606AT[12]	NM_001199398.1:c.2456-7606AT[13]	NM_001199398.1:c.2456-7591_2456-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199398.1:c.2456-7606AT[14]	NM_001199398.1:c.2456-7606AT[15]	NM_001199398.1:c.2456-7606AT[16]	NM_001199398.1:c.2456-7606AT[17]	NM_001199398.1:c.2456-7606AT[18]	NM_001199398.1:c.2456-7606AT[19]
NEK1 transcript variant 3	NM_001199398.3:c.2456-7591=	NM_001199398.3:c.2456-7606AT[5]	NM_001199398.3:c.2456-7606AT[6]	NM_001199398.3:c.2456-7606AT[7]	NM_001199398.3:c.2456-7606AT[9]	NM_001199398.3:c.2456-7606AT[10]	NM_001199398.3:c.2456-7606AT[11]	NM_001199398.3:c.2456-7606AT[12]	NM_001199398.3:c.2456-7606AT[13]	NM_001199398.3:c.2456-7591_2456-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199398.3:c.2456-7606AT[14]	NM_001199398.3:c.2456-7606AT[15]	NM_001199398.3:c.2456-7606AT[16]	NM_001199398.3:c.2456-7606AT[17]	NM_001199398.3:c.2456-7606AT[18]	NM_001199398.3:c.2456-7606AT[19]
NEK1 transcript variant 4	NM_001199399.1:c.2297-7591=	NM_001199399.1:c.2297-7606AT[5]	NM_001199399.1:c.2297-7606AT[6]	NM_001199399.1:c.2297-7606AT[7]	NM_001199399.1:c.2297-7606AT[9]	NM_001199399.1:c.2297-7606AT[10]	NM_001199399.1:c.2297-7606AT[11]	NM_001199399.1:c.2297-7606AT[12]	NM_001199399.1:c.2297-7606AT[13]	NM_001199399.1:c.2297-7591_2297-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199399.1:c.2297-7606AT[14]	NM_001199399.1:c.2297-7606AT[15]	NM_001199399.1:c.2297-7606AT[16]	NM_001199399.1:c.2297-7606AT[17]	NM_001199399.1:c.2297-7606AT[18]	NM_001199399.1:c.2297-7606AT[19]
NEK1 transcript variant 4	NM_001199399.3:c.2297-7591=	NM_001199399.3:c.2297-7606AT[5]	NM_001199399.3:c.2297-7606AT[6]	NM_001199399.3:c.2297-7606AT[7]	NM_001199399.3:c.2297-7606AT[9]	NM_001199399.3:c.2297-7606AT[10]	NM_001199399.3:c.2297-7606AT[11]	NM_001199399.3:c.2297-7606AT[12]	NM_001199399.3:c.2297-7606AT[13]	NM_001199399.3:c.2297-7591_2297-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199399.3:c.2297-7606AT[14]	NM_001199399.3:c.2297-7606AT[15]	NM_001199399.3:c.2297-7606AT[16]	NM_001199399.3:c.2297-7606AT[17]	NM_001199399.3:c.2297-7606AT[18]	NM_001199399.3:c.2297-7606AT[19]
NEK1 transcript variant 5	NM_001199400.1:c.2372-7591=	NM_001199400.1:c.2372-7606AT[5]	NM_001199400.1:c.2372-7606AT[6]	NM_001199400.1:c.2372-7606AT[7]	NM_001199400.1:c.2372-7606AT[9]	NM_001199400.1:c.2372-7606AT[10]	NM_001199400.1:c.2372-7606AT[11]	NM_001199400.1:c.2372-7606AT[12]	NM_001199400.1:c.2372-7606AT[13]	NM_001199400.1:c.2372-7591_2372-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199400.1:c.2372-7606AT[14]	NM_001199400.1:c.2372-7606AT[15]	NM_001199400.1:c.2372-7606AT[16]	NM_001199400.1:c.2372-7606AT[17]	NM_001199400.1:c.2372-7606AT[18]	NM_001199400.1:c.2372-7606AT[19]
NEK1 transcript variant 5	NM_001199400.3:c.2372-7591=	NM_001199400.3:c.2372-7606AT[5]	NM_001199400.3:c.2372-7606AT[6]	NM_001199400.3:c.2372-7606AT[7]	NM_001199400.3:c.2372-7606AT[9]	NM_001199400.3:c.2372-7606AT[10]	NM_001199400.3:c.2372-7606AT[11]	NM_001199400.3:c.2372-7606AT[12]	NM_001199400.3:c.2372-7606AT[13]	NM_001199400.3:c.2372-7591_2372-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001199400.3:c.2372-7606AT[14]	NM_001199400.3:c.2372-7606AT[15]	NM_001199400.3:c.2372-7606AT[16]	NM_001199400.3:c.2372-7606AT[17]	NM_001199400.3:c.2372-7606AT[18]	NM_001199400.3:c.2372-7606AT[19]
NEK1 transcript variant 6	NM_001374418.1:c.2588-7591=	NM_001374418.1:c.2588-7606AT[5]	NM_001374418.1:c.2588-7606AT[6]	NM_001374418.1:c.2588-7606AT[7]	NM_001374418.1:c.2588-7606AT[9]	NM_001374418.1:c.2588-7606AT[10]	NM_001374418.1:c.2588-7606AT[11]	NM_001374418.1:c.2588-7606AT[12]	NM_001374418.1:c.2588-7606AT[13]	NM_001374418.1:c.2588-7591_2588-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001374418.1:c.2588-7606AT[14]	NM_001374418.1:c.2588-7606AT[15]	NM_001374418.1:c.2588-7606AT[16]	NM_001374418.1:c.2588-7606AT[17]	NM_001374418.1:c.2588-7606AT[18]	NM_001374418.1:c.2588-7606AT[19]
NEK1 transcript variant 7	NM_001374419.1:c.2504-7591=	NM_001374419.1:c.2504-7606AT[5]	NM_001374419.1:c.2504-7606AT[6]	NM_001374419.1:c.2504-7606AT[7]	NM_001374419.1:c.2504-7606AT[9]	NM_001374419.1:c.2504-7606AT[10]	NM_001374419.1:c.2504-7606AT[11]	NM_001374419.1:c.2504-7606AT[12]	NM_001374419.1:c.2504-7606AT[13]	NM_001374419.1:c.2504-7591_2504-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001374419.1:c.2504-7606AT[14]	NM_001374419.1:c.2504-7606AT[15]	NM_001374419.1:c.2504-7606AT[16]	NM_001374419.1:c.2504-7606AT[17]	NM_001374419.1:c.2504-7606AT[18]	NM_001374419.1:c.2504-7606AT[19]
NEK1 transcript variant 8	NM_001374420.1:c.2453-7591=	NM_001374420.1:c.2453-7606AT[5]	NM_001374420.1:c.2453-7606AT[6]	NM_001374420.1:c.2453-7606AT[7]	NM_001374420.1:c.2453-7606AT[9]	NM_001374420.1:c.2453-7606AT[10]	NM_001374420.1:c.2453-7606AT[11]	NM_001374420.1:c.2453-7606AT[12]	NM_001374420.1:c.2453-7606AT[13]	NM_001374420.1:c.2453-7591_2453-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001374420.1:c.2453-7606AT[14]	NM_001374420.1:c.2453-7606AT[15]	NM_001374420.1:c.2453-7606AT[16]	NM_001374420.1:c.2453-7606AT[17]	NM_001374420.1:c.2453-7606AT[18]	NM_001374420.1:c.2453-7606AT[19]
NEK1 transcript variant 9	NM_001374421.1:c.2282-12185=	NM_001374421.1:c.2282-12200AT[5]	NM_001374421.1:c.2282-12200AT[6]	NM_001374421.1:c.2282-12200AT[7]	NM_001374421.1:c.2282-12200AT[9]	NM_001374421.1:c.2282-12200AT[10]	NM_001374421.1:c.2282-12200AT[11]	NM_001374421.1:c.2282-12200AT[12]	NM_001374421.1:c.2282-12200AT[13]	NM_001374421.1:c.2282-12185_2282-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_001374421.1:c.2282-12200AT[14]	NM_001374421.1:c.2282-12200AT[15]	NM_001374421.1:c.2282-12200AT[16]	NM_001374421.1:c.2282-12200AT[17]	NM_001374421.1:c.2282-12200AT[18]	NM_001374421.1:c.2282-12200AT[19]
NEK1 transcript variant 2	NM_012224.2:c.2504-7591=	NM_012224.2:c.2504-7606AT[5]	NM_012224.2:c.2504-7606AT[6]	NM_012224.2:c.2504-7606AT[7]	NM_012224.2:c.2504-7606AT[9]	NM_012224.2:c.2504-7606AT[10]	NM_012224.2:c.2504-7606AT[11]	NM_012224.2:c.2504-7606AT[12]	NM_012224.2:c.2504-7606AT[13]	NM_012224.2:c.2504-7591_2504-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_012224.2:c.2504-7606AT[14]	NM_012224.2:c.2504-7606AT[15]	NM_012224.2:c.2504-7606AT[16]	NM_012224.2:c.2504-7606AT[17]	NM_012224.2:c.2504-7606AT[18]	NM_012224.2:c.2504-7606AT[19]
NEK1 transcript variant 2	NM_012224.4:c.2504-7591=	NM_012224.4:c.2504-7606AT[5]	NM_012224.4:c.2504-7606AT[6]	NM_012224.4:c.2504-7606AT[7]	NM_012224.4:c.2504-7606AT[9]	NM_012224.4:c.2504-7606AT[10]	NM_012224.4:c.2504-7606AT[11]	NM_012224.4:c.2504-7606AT[12]	NM_012224.4:c.2504-7606AT[13]	NM_012224.4:c.2504-7591_2504-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	NM_012224.4:c.2504-7606AT[14]	NM_012224.4:c.2504-7606AT[15]	NM_012224.4:c.2504-7606AT[16]	NM_012224.4:c.2504-7606AT[17]	NM_012224.4:c.2504-7606AT[18]	NM_012224.4:c.2504-7606AT[19]
NEK1 transcript variant X1	XM_005263027.1:c.2504-7591=	XM_005263027.1:c.2504-7606AT[5]	XM_005263027.1:c.2504-7606AT[6]	XM_005263027.1:c.2504-7606AT[7]	XM_005263027.1:c.2504-7606AT[9]	XM_005263027.1:c.2504-7606AT[10]	XM_005263027.1:c.2504-7606AT[11]	XM_005263027.1:c.2504-7606AT[12]	XM_005263027.1:c.2504-7606AT[13]	XM_005263027.1:c.2504-7591_2504-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_005263027.1:c.2504-7606AT[14]	XM_005263027.1:c.2504-7606AT[15]	XM_005263027.1:c.2504-7606AT[16]	XM_005263027.1:c.2504-7606AT[17]	XM_005263027.1:c.2504-7606AT[18]	XM_005263027.1:c.2504-7606AT[19]
NEK1 transcript variant X2	XM_005263028.1:c.2372-7591=	XM_005263028.1:c.2372-7606AT[5]	XM_005263028.1:c.2372-7606AT[6]	XM_005263028.1:c.2372-7606AT[7]	XM_005263028.1:c.2372-7606AT[9]	XM_005263028.1:c.2372-7606AT[10]	XM_005263028.1:c.2372-7606AT[11]	XM_005263028.1:c.2372-7606AT[12]	XM_005263028.1:c.2372-7606AT[13]	XM_005263028.1:c.2372-7591_2372-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_005263028.1:c.2372-7606AT[14]	XM_005263028.1:c.2372-7606AT[15]	XM_005263028.1:c.2372-7606AT[16]	XM_005263028.1:c.2372-7606AT[17]	XM_005263028.1:c.2372-7606AT[18]	XM_005263028.1:c.2372-7606AT[19]
NEK1 transcript variant X3	XM_011532004.2:c.2372-7591=	XM_011532004.2:c.2372-7606AT[5]	XM_011532004.2:c.2372-7606AT[6]	XM_011532004.2:c.2372-7606AT[7]	XM_011532004.2:c.2372-7606AT[9]	XM_011532004.2:c.2372-7606AT[10]	XM_011532004.2:c.2372-7606AT[11]	XM_011532004.2:c.2372-7606AT[12]	XM_011532004.2:c.2372-7606AT[13]	XM_011532004.2:c.2372-7591_2372-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_011532004.2:c.2372-7606AT[14]	XM_011532004.2:c.2372-7606AT[15]	XM_011532004.2:c.2372-7606AT[16]	XM_011532004.2:c.2372-7606AT[17]	XM_011532004.2:c.2372-7606AT[18]	XM_011532004.2:c.2372-7606AT[19]
NEK1 transcript variant X1	XM_047415731.1:c.2456-7591=	XM_047415731.1:c.2456-7606AT[5]	XM_047415731.1:c.2456-7606AT[6]	XM_047415731.1:c.2456-7606AT[7]	XM_047415731.1:c.2456-7606AT[9]	XM_047415731.1:c.2456-7606AT[10]	XM_047415731.1:c.2456-7606AT[11]	XM_047415731.1:c.2456-7606AT[12]	XM_047415731.1:c.2456-7606AT[13]	XM_047415731.1:c.2456-7591_2456-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415731.1:c.2456-7606AT[14]	XM_047415731.1:c.2456-7606AT[15]	XM_047415731.1:c.2456-7606AT[16]	XM_047415731.1:c.2456-7606AT[17]	XM_047415731.1:c.2456-7606AT[18]	XM_047415731.1:c.2456-7606AT[19]
NEK1 transcript variant X2	XM_047415732.1:c.2588-12185=	XM_047415732.1:c.2588-12200AT[5]	XM_047415732.1:c.2588-12200AT[6]	XM_047415732.1:c.2588-12200AT[7]	XM_047415732.1:c.2588-12200AT[9]	XM_047415732.1:c.2588-12200AT[10]	XM_047415732.1:c.2588-12200AT[11]	XM_047415732.1:c.2588-12200AT[12]	XM_047415732.1:c.2588-12200AT[13]	XM_047415732.1:c.2588-12185_2588-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415732.1:c.2588-12200AT[14]	XM_047415732.1:c.2588-12200AT[15]	XM_047415732.1:c.2588-12200AT[16]	XM_047415732.1:c.2588-12200AT[17]	XM_047415732.1:c.2588-12200AT[18]	XM_047415732.1:c.2588-12200AT[19]
NEK1 transcript variant X4	XM_047415733.1:c.2504-12185=	XM_047415733.1:c.2504-12200AT[5]	XM_047415733.1:c.2504-12200AT[6]	XM_047415733.1:c.2504-12200AT[7]	XM_047415733.1:c.2504-12200AT[9]	XM_047415733.1:c.2504-12200AT[10]	XM_047415733.1:c.2504-12200AT[11]	XM_047415733.1:c.2504-12200AT[12]	XM_047415733.1:c.2504-12200AT[13]	XM_047415733.1:c.2504-12185_2504-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415733.1:c.2504-12200AT[14]	XM_047415733.1:c.2504-12200AT[15]	XM_047415733.1:c.2504-12200AT[16]	XM_047415733.1:c.2504-12200AT[17]	XM_047415733.1:c.2504-12200AT[18]	XM_047415733.1:c.2504-12200AT[19]
NEK1 transcript variant X5	XM_047415734.1:c.2504-12185=	XM_047415734.1:c.2504-12200AT[5]	XM_047415734.1:c.2504-12200AT[6]	XM_047415734.1:c.2504-12200AT[7]	XM_047415734.1:c.2504-12200AT[9]	XM_047415734.1:c.2504-12200AT[10]	XM_047415734.1:c.2504-12200AT[11]	XM_047415734.1:c.2504-12200AT[12]	XM_047415734.1:c.2504-12200AT[13]	XM_047415734.1:c.2504-12185_2504-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415734.1:c.2504-12200AT[14]	XM_047415734.1:c.2504-12200AT[15]	XM_047415734.1:c.2504-12200AT[16]	XM_047415734.1:c.2504-12200AT[17]	XM_047415734.1:c.2504-12200AT[18]	XM_047415734.1:c.2504-12200AT[19]
NEK1 transcript variant X6	XM_047415735.1:c.2456-12185=	XM_047415735.1:c.2456-12200AT[5]	XM_047415735.1:c.2456-12200AT[6]	XM_047415735.1:c.2456-12200AT[7]	XM_047415735.1:c.2456-12200AT[9]	XM_047415735.1:c.2456-12200AT[10]	XM_047415735.1:c.2456-12200AT[11]	XM_047415735.1:c.2456-12200AT[12]	XM_047415735.1:c.2456-12200AT[13]	XM_047415735.1:c.2456-12185_2456-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415735.1:c.2456-12200AT[14]	XM_047415735.1:c.2456-12200AT[15]	XM_047415735.1:c.2456-12200AT[16]	XM_047415735.1:c.2456-12200AT[17]	XM_047415735.1:c.2456-12200AT[18]	XM_047415735.1:c.2456-12200AT[19]
NEK1 transcript variant X7	XM_047415736.1:c.2372-12185=	XM_047415736.1:c.2372-12200AT[5]	XM_047415736.1:c.2372-12200AT[6]	XM_047415736.1:c.2372-12200AT[7]	XM_047415736.1:c.2372-12200AT[9]	XM_047415736.1:c.2372-12200AT[10]	XM_047415736.1:c.2372-12200AT[11]	XM_047415736.1:c.2372-12200AT[12]	XM_047415736.1:c.2372-12200AT[13]	XM_047415736.1:c.2372-12185_2372-12184insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415736.1:c.2372-12200AT[14]	XM_047415736.1:c.2372-12200AT[15]	XM_047415736.1:c.2372-12200AT[16]	XM_047415736.1:c.2372-12200AT[17]	XM_047415736.1:c.2372-12200AT[18]	XM_047415736.1:c.2372-12200AT[19]
NEK1 transcript variant X8	XM_047415737.1:c.1967-7591=	XM_047415737.1:c.1967-7606AT[5]	XM_047415737.1:c.1967-7606AT[6]	XM_047415737.1:c.1967-7606AT[7]	XM_047415737.1:c.1967-7606AT[9]	XM_047415737.1:c.1967-7606AT[10]	XM_047415737.1:c.1967-7606AT[11]	XM_047415737.1:c.1967-7606AT[12]	XM_047415737.1:c.1967-7606AT[13]	XM_047415737.1:c.1967-7591_1967-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415737.1:c.1967-7606AT[14]	XM_047415737.1:c.1967-7606AT[15]	XM_047415737.1:c.1967-7606AT[16]	XM_047415737.1:c.1967-7606AT[17]	XM_047415737.1:c.1967-7606AT[18]	XM_047415737.1:c.1967-7606AT[19]
NEK1 transcript variant X9	XM_047415738.1:c.1967-7591=	XM_047415738.1:c.1967-7606AT[5]	XM_047415738.1:c.1967-7606AT[6]	XM_047415738.1:c.1967-7606AT[7]	XM_047415738.1:c.1967-7606AT[9]	XM_047415738.1:c.1967-7606AT[10]	XM_047415738.1:c.1967-7606AT[11]	XM_047415738.1:c.1967-7606AT[12]	XM_047415738.1:c.1967-7606AT[13]	XM_047415738.1:c.1967-7591_1967-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415738.1:c.1967-7606AT[14]	XM_047415738.1:c.1967-7606AT[15]	XM_047415738.1:c.1967-7606AT[16]	XM_047415738.1:c.1967-7606AT[17]	XM_047415738.1:c.1967-7606AT[18]	XM_047415738.1:c.1967-7606AT[19]
NEK1 transcript variant X10	XM_047415739.1:c.1883-7591=	XM_047415739.1:c.1883-7606AT[5]	XM_047415739.1:c.1883-7606AT[6]	XM_047415739.1:c.1883-7606AT[7]	XM_047415739.1:c.1883-7606AT[9]	XM_047415739.1:c.1883-7606AT[10]	XM_047415739.1:c.1883-7606AT[11]	XM_047415739.1:c.1883-7606AT[12]	XM_047415739.1:c.1883-7606AT[13]	XM_047415739.1:c.1883-7591_1883-7590insTATATATATATATATATATATATATATATATATATGTATATATATA	XM_047415739.1:c.1883-7606AT[14]	XM_047415739.1:c.1883-7606AT[15]	XM_047415739.1:c.1883-7606AT[16]	XM_047415739.1:c.1883-7606AT[17]	XM_047415739.1:c.1883-7606AT[18]	XM_047415739.1:c.1883-7606AT[19]

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#.

68 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95377813	Feb 13, 2009 (130)
2	GMI	ss288596407	May 04, 2012 (137)
3	1000GENOMES	ss326606579	May 09, 2011 (134)
4	1000GENOMES	ss326643386	May 09, 2011 (134)
5	LUNTER	ss551444661	Apr 25, 2013 (138)
6	LUNTER	ss551584595	Apr 25, 2013 (138)
7	LUNTER	ss553175359	Apr 25, 2013 (138)
8	SSMP	ss663480624	Apr 01, 2015 (144)
9	BILGI_BIOE	ss666288666	Apr 25, 2013 (138)
10	DDI	ss1536440635	Apr 01, 2015 (144)
11	EVA_GENOME_DK	ss1576397729	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1704465305	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1704465307	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1704467002	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1704467005	Apr 01, 2015 (144)
16	SWEGEN	ss2996007916	Jan 10, 2018 (151)
17	MCHAISSO	ss3065989123	Nov 08, 2017 (151)
18	URBANLAB	ss3647915551	Oct 12, 2018 (152)
19	EVA_DECODE	ss3713608319	Jul 13, 2019 (153)
20	EVA_DECODE	ss3713608320	Jul 13, 2019 (153)
21	EVA_DECODE	ss3713608321	Jul 13, 2019 (153)
22	EVA_DECODE	ss3713608322	Jul 13, 2019 (153)
23	EVA_DECODE	ss3713608323	Jul 13, 2019 (153)
24	ACPOP	ss3731854444	Jul 13, 2019 (153)
25	ACPOP	ss3731854445	Jul 13, 2019 (153)
26	PACBIO	ss3784942187	Jul 13, 2019 (153)
27	PACBIO	ss3790367096	Jul 13, 2019 (153)
28	PACBIO	ss3795242780	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3805915826	Jul 13, 2019 (153)
30	GNOMAD	ss4125275839	Apr 26, 2021 (155)
31	GNOMAD	ss4125275841	Apr 26, 2021 (155)
32	GNOMAD	ss4125275842	Apr 26, 2021 (155)
33	GNOMAD	ss4125275843	Apr 26, 2021 (155)
34	GNOMAD	ss4125275844	Apr 26, 2021 (155)
35	GNOMAD	ss4125275845	Apr 26, 2021 (155)
36	GNOMAD	ss4125275846	Apr 26, 2021 (155)
37	GNOMAD	ss4125275847	Apr 26, 2021 (155)
38	GNOMAD	ss4125275848	Apr 26, 2021 (155)
39	GNOMAD	ss4125275849	Apr 26, 2021 (155)
40	GNOMAD	ss4125275850	Apr 26, 2021 (155)
41	GNOMAD	ss4125275851	Apr 26, 2021 (155)
42	GNOMAD	ss4125275854	Apr 26, 2021 (155)
43	GNOMAD	ss4125275855	Apr 26, 2021 (155)
44	GNOMAD	ss4125275856	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5169265007	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5169265008	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5169265009	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5169265010	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5262001003	Oct 17, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5262001004	Oct 17, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5262001005	Oct 17, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5262001006	Oct 17, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5262001007	Oct 17, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5262001008	Oct 17, 2022 (156)
55	HUGCELL_USP	ss5460450850	Oct 17, 2022 (156)
56	HUGCELL_USP	ss5460450851	Oct 17, 2022 (156)
57	HUGCELL_USP	ss5460450852	Oct 17, 2022 (156)
58	HUGCELL_USP	ss5460450853	Oct 17, 2022 (156)
59	HUGCELL_USP	ss5460450854	Oct 17, 2022 (156)
60	HUGCELL_USP	ss5460450855	Oct 17, 2022 (156)
61	TOMMO_GENOMICS	ss5704604009	Oct 17, 2022 (156)
62	TOMMO_GENOMICS	ss5704604010	Oct 17, 2022 (156)
63	TOMMO_GENOMICS	ss5704604011	Oct 17, 2022 (156)
64	TOMMO_GENOMICS	ss5704604013	Oct 17, 2022 (156)
65	TOMMO_GENOMICS	ss5704604014	Oct 17, 2022 (156)
66	EVA	ss5845100844	Oct 17, 2022 (156)
67	EVA	ss5845100845	Oct 17, 2022 (156)
68	EVA	ss5854564706	Oct 17, 2022 (156)
69	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 13599324 (NC_000004.11:170367000::AT 2047/3854) Row 13599325 (NC_000004.11:170367000::ATAT 556/3854)	-	Oct 12, 2018 (152)
70	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 13599324 (NC_000004.11:170367000::AT 2047/3854) Row 13599325 (NC_000004.11:170367000::ATAT 556/3854)	-	Oct 12, 2018 (152)
71	The Danish reference pan genome	NC_000004.11 - 170367001	Apr 26, 2020 (154)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 173108212 (NC_000004.12:169445849::AT 54030/128312) Row 173108214 (NC_000004.12:169445849::ATAT 6383/128476) Row 173108215 (NC_000004.12:169445849::ATATAT 1338/128536)...	-	Apr 26, 2021 (155)
87	Northern Sweden Submission ignored due to conflicting rows: Row 5139309 (NC_000004.11:170367000::ATAT 12/600) Row 5139310 (NC_000004.11:170367000::AT 338/600)	-	Jul 13, 2019 (153)
88	Northern Sweden Submission ignored due to conflicting rows: Row 5139309 (NC_000004.11:170367000::ATAT 12/600) Row 5139310 (NC_000004.11:170367000::AT 338/600)	-	Jul 13, 2019 (153)
89	8.3KJPN Submission ignored due to conflicting rows: Row 27234314 (NC_000004.11:170367000::AT 12711/16760) Row 27234315 (NC_000004.11:170367000::ATAT 284/16760) Row 27234316 (NC_000004.11:170367000::ATATAT 3/16760)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 27234314 (NC_000004.11:170367000::AT 12711/16760) Row 27234315 (NC_000004.11:170367000::ATAT 284/16760) Row 27234316 (NC_000004.11:170367000::ATATAT 3/16760)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 27234314 (NC_000004.11:170367000::AT 12711/16760) Row 27234315 (NC_000004.11:170367000::ATAT 284/16760) Row 27234316 (NC_000004.11:170367000::ATATAT 3/16760)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 27234314 (NC_000004.11:170367000::AT 12711/16760) Row 27234315 (NC_000004.11:170367000::ATAT 284/16760) Row 27234316 (NC_000004.11:170367000::ATATAT 3/16760)...	-	Apr 26, 2021 (155)
93	14KJPN Submission ignored due to conflicting rows: Row 38441113 (NC_000004.12:169445849::AT 21401/28258) Row 38441114 (NC_000004.12:169445849::ATAT 478/28258) Row 38441115 (NC_000004.12:169445849::ATATAT 4/28258)...	-	Oct 17, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 38441113 (NC_000004.12:169445849::AT 21401/28258) Row 38441114 (NC_000004.12:169445849::ATAT 478/28258) Row 38441115 (NC_000004.12:169445849::ATATAT 4/28258)...	-	Oct 17, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 38441113 (NC_000004.12:169445849::AT 21401/28258) Row 38441114 (NC_000004.12:169445849::ATAT 478/28258) Row 38441115 (NC_000004.12:169445849::ATATAT 4/28258)...	-	Oct 17, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 38441113 (NC_000004.12:169445849::AT 21401/28258) Row 38441114 (NC_000004.12:169445849::ATAT 478/28258) Row 38441115 (NC_000004.12:169445849::ATATAT 4/28258)...	-	Oct 17, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 38441113 (NC_000004.12:169445849::AT 21401/28258) Row 38441114 (NC_000004.12:169445849::ATAT 478/28258) Row 38441115 (NC_000004.12:169445849::ATATAT 4/28258)...	-	Oct 17, 2022 (156)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 13599324 (NC_000004.11:170367000::AT 1982/3708) Row 13599325 (NC_000004.11:170367000::ATAT 543/3708)	-	Oct 12, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 13599324 (NC_000004.11:170367000::AT 1982/3708) Row 13599325 (NC_000004.11:170367000::ATAT 543/3708)	-	Oct 12, 2018 (152)
100	ALFA	NC_000004.12 - 169445850	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)
rs370908652	May 15, 2013 (138)
rs925884686	Nov 08, 2017 (151)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4125275856	NC_000004.12:169445849:ATATAT:	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATA	(self)
ss3713608323, ss4125275855	NC_000004.12:169445849:ATAT:	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATA	(self)
ss2996007916, ss5169265010	NC_000004.11:170367000:AT:	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATA	(self)
ss4125275854, ss5704604013	NC_000004.12:169445849:AT:	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATA	(self)
ss3713608322	NC_000004.12:169445851:AT:	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATA	(self)
ss326606579, ss326643386, ss551444661, ss553175359	NC_000004.10:170603575::AT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss288596407	NC_000004.10:170603592::TA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
961810, ss663480624, ss666288666, ss1536440635, ss1576397729, ss1704465305, ss1704467002, ss3731854445, ss3784942187, ss3790367096, ss3795242780, ss5169265007, ss5845100844	NC_000004.11:170367000::AT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss3805915826, ss4125275839, ss5262001003, ss5460450850, ss5704604009, ss5854564706	NC_000004.12:169445849::AT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss3713608321	NC_000004.12:169445853::AT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATA	(self)
ss551584595	NC_000004.10:170603575::ATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss1704465307, ss1704467005, ss3731854444, ss5169265008, ss5845100845	NC_000004.11:170367000::ATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3647915551, ss4125275841, ss5262001007, ss5460450851, ss5704604010	NC_000004.12:169445849::ATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss3713608320	NC_000004.12:169445853::ATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss95377813	NT_016354.19:94914738::TATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATA	(self)
ss5169265009	NC_000004.11:170367000::ATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss3065989123, ss4125275842, ss5262001004, ss5460450852, ss5704604011	NC_000004.12:169445849::ATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss3713608319	NC_000004.12:169445853::ATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATA	(self)
ss4125275843, ss5262001005, ss5460450853, ss5704604014	NC_000004.12:169445849::ATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATA	(self)
ss4125275844, ss5262001008, ss5460450854	NC_000004.12:169445849::ATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATA	(self)
ss4125275851	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATATATATATATATATACATATATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATACATATATATATATATATATATATATATATATATATA	(self)
ss4125275845, ss5262001006, ss5460450855	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATA	(self)
ss4125275846	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATA	(self)
ss4125275847	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATA	(self)
ss4125275848	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATA	(self)
ss4125275849	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA	(self)
ss4125275850	NC_000004.12:169445849::ATATATATAT… NC_000004.12:169445849::ATATATATATATATATATATAT	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA	(self)
189055580	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA	NC_000004.12:169445849:ATATATATATA… NC_000004.12:169445849:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA	(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 rs70964204

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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs70964204