Name: rs1491231212
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.

rs1491231212

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:73905992-73905995 (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: ins(TA)₁₄TGTATA / ins(TA)₁₃TGTATA …
ins(TA)₁₄TGTATA / ins(TA)₁₃TGTATA / ins(TA)₁₂TGTATA / ins(TA)₁₁TGTATA / ins(TA)₁₀TGTATA / ins(TA)₉TGTATA / ins(TA)₉TGTGTATA / ins(TA)₈TGTATA / ins(TA)₇TGTATA / ins(TA)₆TGTATA / ins(TA)₅TGTATA / ins(TA)₄TGTATA / ins(TA)₃TGTATA / insTATATGTATA / insTATGTATA / insTATG(TA)₅TGTATA / insTGTATA
Variation Type: Indel Insertion and Deletion
Frequency: ins(TA)₇TGTATA=0.00141 (23/16282, ALFA)
ins(TA)₇TGTATA=0.002 (1/600, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF410 : 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	16282	TATA=0.99644	TATATATATATATATATATATGTATA=0.00049, TATATATATATATATATATGTATA=0.00141, TATATATATATATATATGTATA=0.00117, TATATATATATATATGTATA=0.00006, TATATATATATATGTATA=0.00043, TATATATATATGTATA=0.00000, TATATATATGTATA=0.00000, TATATATGTATA=0.00000, TATATGTATA=0.00000	0.997407	0.000123	0.00247	34
European	Sub	12052	TATA=0.99519	TATATATATATATATATATATGTATA=0.00066, TATATATATATATATATATGTATA=0.00191, TATATATATATATATATGTATA=0.00158, TATATATATATATATGTATA=0.00008, TATATATATATATGTATA=0.00058, TATATATATATGTATA=0.00000, TATATATATGTATA=0.00000, TATATATGTATA=0.00000, TATATGTATA=0.00000	0.99649	0.000167	0.003343	25
African	Sub	2798	TATA=1.0000	TATATATATATATATATATATGTATA=0.0000, TATATATATATATATATATGTATA=0.0000, TATATATATATATATATGTATA=0.0000, TATATATATATATATGTATA=0.0000, TATATATATATATGTATA=0.0000, TATATATATATGTATA=0.0000, TATATATATGTATA=0.0000, TATATATGTATA=0.0000, TATATGTATA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	108	TATA=1.000	TATATATATATATATATATATGTATA=0.000, TATATATATATATATATATGTATA=0.000, TATATATATATATATATGTATA=0.000, TATATATATATATATGTATA=0.000, TATATATATATATGTATA=0.000, TATATATATATGTATA=0.000, TATATATATGTATA=0.000, TATATATGTATA=0.000, TATATGTATA=0.000	1.0	0.0	0.0	N/A
African American	Sub	2690	TATA=1.0000	TATATATATATATATATATATGTATA=0.0000, TATATATATATATATATATGTATA=0.0000, TATATATATATATATATGTATA=0.0000, TATATATATATATATGTATA=0.0000, TATATATATATATGTATA=0.0000, TATATATATATGTATA=0.0000, TATATATATGTATA=0.0000, TATATATGTATA=0.0000, TATATGTATA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	108	TATA=1.000	TATATATATATATATATATATGTATA=0.000, TATATATATATATATATATGTATA=0.000, TATATATATATATATATGTATA=0.000, TATATATATATATATGTATA=0.000, TATATATATATATGTATA=0.000, TATATATATATGTATA=0.000, TATATATATGTATA=0.000, TATATATGTATA=0.000, TATATGTATA=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	TATA=1.00	TATATATATATATATATATATGTATA=0.00, TATATATATATATATATATGTATA=0.00, TATATATATATATATATGTATA=0.00, TATATATATATATATGTATA=0.00, TATATATATATATGTATA=0.00, TATATATATATGTATA=0.00, TATATATATGTATA=0.00, TATATATGTATA=0.00, TATATGTATA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	TATA=1.00	TATATATATATATATATATATGTATA=0.00, TATATATATATATATATATGTATA=0.00, TATATATATATATATATGTATA=0.00, TATATATATATATATGTATA=0.00, TATATATATATATGTATA=0.00, TATATATATATGTATA=0.00, TATATATATGTATA=0.00, TATATATGTATA=0.00, TATATGTATA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	144	TATA=1.000	TATATATATATATATATATATGTATA=0.000, TATATATATATATATATATGTATA=0.000, TATATATATATATATATGTATA=0.000, TATATATATATATATGTATA=0.000, TATATATATATATGTATA=0.000, TATATATATATGTATA=0.000, TATATATATGTATA=0.000, TATATATGTATA=0.000, TATATGTATA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	610	TATA=1.000	TATATATATATATATATATATGTATA=0.000, TATATATATATATATATATGTATA=0.000, TATATATATATATATATGTATA=0.000, TATATATATATATATGTATA=0.000, TATATATATATATGTATA=0.000, TATATATATATGTATA=0.000, TATATATATGTATA=0.000, TATATATGTATA=0.000, TATATGTATA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	94	TATA=1.00	TATATATATATATATATATATGTATA=0.00, TATATATATATATATATATGTATA=0.00, TATATATATATATATATGTATA=0.00, TATATATATATATATGTATA=0.00, TATATATATATATGTATA=0.00, TATATATATATGTATA=0.00, TATATATATGTATA=0.00, TATATATGTATA=0.00, TATATGTATA=0.00	1.0	0.0	0.0	N/A
Other	Sub	476	TATA=1.000	TATATATATATATATATATATGTATA=0.000, TATATATATATATATATATGTATA=0.000, TATATATATATATATATGTATA=0.000, TATATATATATATATGTATA=0.000, TATATATATATATGTATA=0.000, TATATATATATGTATA=0.000, TATATATATGTATA=0.000, TATATATGTATA=0.000, TATATGTATA=0.000	1.0	0.0	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
Allele Frequency Aggregator	Total	Global	16282	TATA=0.99644	ins(TA)₈TGTATA=0.00049, ins(TA)₇TGTATA=0.00141, ins(TA)₆TGTATA=0.00117, ins(TA)₅TGTATA=0.00006, ins(TA)₄TGTATA=0.00043, ins(TA)₃TGTATA=0.00000, insTATATGTATA=0.00000, insTATGTATA=0.00000, insTGTATA=0.00000
Allele Frequency Aggregator	European	Sub	12052	TATA=0.99519	ins(TA)₈TGTATA=0.00066, ins(TA)₇TGTATA=0.00191, ins(TA)₆TGTATA=0.00158, ins(TA)₅TGTATA=0.00008, ins(TA)₄TGTATA=0.00058, ins(TA)₃TGTATA=0.00000, insTATATGTATA=0.00000, insTATGTATA=0.00000, insTGTATA=0.00000
Allele Frequency Aggregator	African	Sub	2798	TATA=1.0000	ins(TA)₈TGTATA=0.0000, ins(TA)₇TGTATA=0.0000, ins(TA)₆TGTATA=0.0000, ins(TA)₅TGTATA=0.0000, ins(TA)₄TGTATA=0.0000, ins(TA)₃TGTATA=0.0000, insTATATGTATA=0.0000, insTATGTATA=0.0000, insTGTATA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	TATA=1.000	ins(TA)₈TGTATA=0.000, ins(TA)₇TGTATA=0.000, ins(TA)₆TGTATA=0.000, ins(TA)₅TGTATA=0.000, ins(TA)₄TGTATA=0.000, ins(TA)₃TGTATA=0.000, insTATATGTATA=0.000, insTATGTATA=0.000, insTGTATA=0.000
Allele Frequency Aggregator	Other	Sub	476	TATA=1.000	ins(TA)₈TGTATA=0.000, ins(TA)₇TGTATA=0.000, ins(TA)₆TGTATA=0.000, ins(TA)₅TGTATA=0.000, ins(TA)₄TGTATA=0.000, ins(TA)₃TGTATA=0.000, insTATATGTATA=0.000, insTATGTATA=0.000, insTGTATA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	TATA=1.000	ins(TA)₈TGTATA=0.000, ins(TA)₇TGTATA=0.000, ins(TA)₆TGTATA=0.000, ins(TA)₅TGTATA=0.000, ins(TA)₄TGTATA=0.000, ins(TA)₃TGTATA=0.000, insTATATGTATA=0.000, insTATGTATA=0.000, insTGTATA=0.000
Allele Frequency Aggregator	Asian	Sub	108	TATA=1.000	ins(TA)₈TGTATA=0.000, ins(TA)₇TGTATA=0.000, ins(TA)₆TGTATA=0.000, ins(TA)₅TGTATA=0.000, ins(TA)₄TGTATA=0.000, ins(TA)₃TGTATA=0.000, insTATATGTATA=0.000, insTATGTATA=0.000, insTGTATA=0.000
Allele Frequency Aggregator	South Asian	Sub	94	TATA=1.00	ins(TA)₈TGTATA=0.00, ins(TA)₇TGTATA=0.00, ins(TA)₆TGTATA=0.00, ins(TA)₅TGTATA=0.00, ins(TA)₄TGTATA=0.00, ins(TA)₃TGTATA=0.00, insTATATGTATA=0.00, insTATGTATA=0.00, insTGTATA=0.00
Northern Sweden	ACPOP	Study-wide	600	- No frequency provided	ins(TA)₇TGTATA=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 14	NC_000014.9:g.73905992_73905995TA[16]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[15]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[14]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[13]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[12]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[11]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[11]TG[2]TA[2]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[10]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[9]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[8]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[7]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[6]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[5]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[4]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[3]TGTATA[1]
GRCh38.p14 chr 14	NC_000014.9:g.73905995_73905996insTATGTATATATATATGTATA
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995TA[2]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[16]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[15]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[14]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[13]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[12]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[11]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[11]TG[2]TA[2]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[10]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[9]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[8]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[7]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[6]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[5]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[4]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[3]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372698_74372699insTATGTATATATATATGTATA
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698TA[2]TGTATA[1]

Gene: ZNF410, zinc finger protein 410 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF410 transcript variant 1	NM_001242924.2:c.964+912_… NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATATATATATGTATA	N/A	Intron Variant
ZNF410 transcript variant 3	NM_001242926.2:c.913+912_… NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	N/A	Intron Variant
ZNF410 transcript variant 4	NM_001242927.2:c.694+912_… NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATATATATATGTATA	N/A	Intron Variant
ZNF410 transcript variant 5	NM_001242928.2:c.325+912_… NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATATATATATGTATA	N/A	Intron Variant
ZNF410 transcript variant 2	NM_021188.3:c.913+912_913… NM_021188.3:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	N/A	Intron Variant
ZNF410 transcript variant 6	NR_040251.2:n.	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	TATA=	ins(TA)₁₄TGTATA	ins(TA)₁₃TGTATA	ins(TA)₁₂TGTATA	ins(TA)₁₁TGTATA	ins(TA)₁₀TGTATA	ins(TA)₉TGTATA	ins(TA)₉TGTGTATA	ins(TA)₈TGTATA	ins(TA)₇TGTATA	ins(TA)₆TGTATA	ins(TA)₅TGTATA	ins(TA)₄TGTATA	ins(TA)₃TGTATA	insTATATGTATA	insTATGTATA	insTATG(TA)₅TGTATA	insTGTATA
GRCh38.p14 chr 14	NC_000014.9:g.73905992_73905995=	NC_000014.9:g.73905992_73905995TA[16]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[15]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[14]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[13]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[12]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[11]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[11]TG[2]TA[2]	NC_000014.9:g.73905992_73905995TA[10]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[9]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[8]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[7]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[6]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[5]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[4]TGTATA[1]	NC_000014.9:g.73905992_73905995TA[3]TGTATA[1]	NC_000014.9:g.73905995_73905996insTATGTATATATATATGTATA	NC_000014.9:g.73905992_73905995TA[2]TGTATA[1]
GRCh37.p13 chr 14	NC_000014.8:g.74372695_74372698=	NC_000014.8:g.74372695_74372698TA[16]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[15]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[14]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[13]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[12]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[11]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[11]TG[2]TA[2]	NC_000014.8:g.74372695_74372698TA[10]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[9]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[8]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[7]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[6]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[5]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[4]TGTATA[1]	NC_000014.8:g.74372695_74372698TA[3]TGTATA[1]	NC_000014.8:g.74372698_74372699insTATGTATATATATATGTATA	NC_000014.8:g.74372695_74372698TA[2]TGTATA[1]
ZNF410 transcript variant 1	NM_001242924.1:c.964+909=	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATATGTGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATATGTATA	NM_001242924.1:c.964+912_964+913insTATATGTATA	NM_001242924.1:c.964+912_964+913insTATGTATA	NM_001242924.1:c.964+912_964+913insTATGTATATATATATGTATA	NM_001242924.1:c.964+912_964+913insTGTATA
ZNF410 transcript variant 1	NM_001242924.2:c.964+909=	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATATGTGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATATGTATA	NM_001242924.2:c.964+912_964+913insTATATGTATA	NM_001242924.2:c.964+912_964+913insTATGTATA	NM_001242924.2:c.964+912_964+913insTATGTATATATATATGTATA	NM_001242924.2:c.964+912_964+913insTGTATA
ZNF410 transcript variant 3	NM_001242926.1:c.913+909=	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATATGTGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATATGTATA	NM_001242926.1:c.913+912_913+913insTATATGTATA	NM_001242926.1:c.913+912_913+913insTATGTATA	NM_001242926.1:c.913+912_913+913insTATGTATATATATATGTATA	NM_001242926.1:c.913+912_913+913insTGTATA
ZNF410 transcript variant 3	NM_001242926.2:c.913+909=	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATATGTGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATATGTATA	NM_001242926.2:c.913+912_913+913insTATATGTATA	NM_001242926.2:c.913+912_913+913insTATGTATA	NM_001242926.2:c.913+912_913+913insTATGTATATATATATGTATA	NM_001242926.2:c.913+912_913+913insTGTATA
ZNF410 transcript variant 4	NM_001242927.1:c.694+909=	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATATGTGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATATGTATA	NM_001242927.1:c.694+912_694+913insTATATGTATA	NM_001242927.1:c.694+912_694+913insTATGTATA	NM_001242927.1:c.694+912_694+913insTATGTATATATATATGTATA	NM_001242927.1:c.694+912_694+913insTGTATA
ZNF410 transcript variant 4	NM_001242927.2:c.694+909=	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATATGTGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATATGTATA	NM_001242927.2:c.694+912_694+913insTATATGTATA	NM_001242927.2:c.694+912_694+913insTATGTATA	NM_001242927.2:c.694+912_694+913insTATGTATATATATATGTATA	NM_001242927.2:c.694+912_694+913insTGTATA
ZNF410 transcript variant 5	NM_001242928.1:c.325+909=	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATATGTGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATATGTATA	NM_001242928.1:c.325+912_325+913insTATATGTATA	NM_001242928.1:c.325+912_325+913insTATGTATA	NM_001242928.1:c.325+912_325+913insTATGTATATATATATGTATA	NM_001242928.1:c.325+912_325+913insTGTATA
ZNF410 transcript variant 5	NM_001242928.2:c.325+909=	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATATGTGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATATGTATA	NM_001242928.2:c.325+912_325+913insTATATGTATA	NM_001242928.2:c.325+912_325+913insTATGTATA	NM_001242928.2:c.325+912_325+913insTATGTATATATATATGTATA	NM_001242928.2:c.325+912_325+913insTGTATA
ZNF410 transcript variant 2	NM_021188.2:c.913+909=	NM_021188.2:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATATGTGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATATGTATA	NM_021188.2:c.913+912_913+913insTATATATGTATA	NM_021188.2:c.913+912_913+913insTATATGTATA	NM_021188.2:c.913+912_913+913insTATGTATA	NM_021188.2:c.913+912_913+913insTATGTATATATATATGTATA	NM_021188.2:c.913+912_913+913insTGTATA
ZNF410 transcript variant 2	NM_021188.3:c.913+909=	NM_021188.3:c.913+912_913+913insTATATATATATATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATATGTGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATATGTATA	NM_021188.3:c.913+912_913+913insTATATATGTATA	NM_021188.3:c.913+912_913+913insTATATGTATA	NM_021188.3:c.913+912_913+913insTATGTATA	NM_021188.3:c.913+912_913+913insTATGTATATATATATGTATA	NM_021188.3:c.913+912_913+913insTGTATA

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#.

36 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3012454777	Jan 10, 2018 (151)
2	SWEGEN	ss3012454778	Jan 10, 2018 (151)
3	SWEGEN	ss3012454779	Jan 10, 2018 (151)
4	SWEGEN	ss3012454781	Jan 10, 2018 (151)
5	ACPOP	ss3740519452	Jul 13, 2019 (153)
6	GNOMAD	ss4280726169	Apr 26, 2021 (155)
7	GNOMAD	ss4280726170	Apr 26, 2021 (155)
8	GNOMAD	ss4280726171	Apr 26, 2021 (155)
9	GNOMAD	ss4280726172	Apr 26, 2021 (155)
10	GNOMAD	ss4280726173	Apr 26, 2021 (155)
11	GNOMAD	ss4280726174	Apr 26, 2021 (155)
12	GNOMAD	ss4280726175	Apr 26, 2021 (155)
13	GNOMAD	ss4280726176	Apr 26, 2021 (155)
14	GNOMAD	ss4280726177	Apr 26, 2021 (155)
15	GNOMAD	ss4280726178	Apr 26, 2021 (155)
16	GNOMAD	ss4280726179	Apr 26, 2021 (155)
17	GNOMAD	ss4280726180	Apr 26, 2021 (155)
18	GNOMAD	ss4280726181	Apr 26, 2021 (155)
19	GNOMAD	ss4280726182	Apr 26, 2021 (155)
20	GNOMAD	ss4280726183	Apr 26, 2021 (155)
21	GNOMAD	ss4280726184	Apr 26, 2021 (155)
22	GNOMAD	ss4280726185	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5213933158	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5213933159	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5213933160	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5213933161	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5213933162	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5296765808	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5296765809	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5490756879	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5490756880	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5766940554	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5766940555	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5766940556	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5766940557	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5766940558	Oct 16, 2022 (156)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 455663353 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG 1/130506) Row 455663354 (NC_000014.9:73905991::TATATATATATATATATATATATATATATATG 1/130504) Row 455663355 (NC_000014.9:73905991::TATATATATATATATATATATATATATATG 7/130496)...	-	Apr 26, 2021 (155)
54	Northern Sweden	NC_000014.8 - 74372695	Jul 13, 2019 (153)
55	8.3KJPN Submission ignored due to conflicting rows: Row 71902465 (NC_000014.8:74372694::TATATATATATATATATG 525/16758) Row 71902466 (NC_000014.8:74372694::TATATATATATATATATATG 357/16758) Row 71902467 (NC_000014.8:74372694::TATATATATATATATG 161/16758)...	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 71902465 (NC_000014.8:74372694::TATATATATATATATATG 525/16758) Row 71902466 (NC_000014.8:74372694::TATATATATATATATATATG 357/16758) Row 71902467 (NC_000014.8:74372694::TATATATATATATATG 161/16758)...	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 71902465 (NC_000014.8:74372694::TATATATATATATATATG 525/16758) Row 71902466 (NC_000014.8:74372694::TATATATATATATATATATG 357/16758) Row 71902467 (NC_000014.8:74372694::TATATATATATATATG 161/16758)...	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 71902465 (NC_000014.8:74372694::TATATATATATATATATG 525/16758) Row 71902466 (NC_000014.8:74372694::TATATATATATATATATATG 357/16758) Row 71902467 (NC_000014.8:74372694::TATATATATATATATG 161/16758)...	-	Apr 26, 2021 (155)
59	8.3KJPN Submission ignored due to conflicting rows: Row 71902465 (NC_000014.8:74372694::TATATATATATATATATG 525/16758) Row 71902466 (NC_000014.8:74372694::TATATATATATATATATATG 357/16758) Row 71902467 (NC_000014.8:74372694::TATATATATATATATG 161/16758)...	-	Apr 26, 2021 (155)
60	14KJPN Submission ignored due to conflicting rows: Row 100777658 (NC_000014.9:73905991::TATATATATATATATATG 869/28218) Row 100777659 (NC_000014.9:73905991::TATATATATATATATATATG 584/28218) Row 100777660 (NC_000014.9:73905991::TATATATATATATATG 289/28218)...	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 100777658 (NC_000014.9:73905991::TATATATATATATATATG 869/28218) Row 100777659 (NC_000014.9:73905991::TATATATATATATATATATG 584/28218) Row 100777660 (NC_000014.9:73905991::TATATATATATATATG 289/28218)...	-	Oct 16, 2022 (156)
62	14KJPN Submission ignored due to conflicting rows: Row 100777658 (NC_000014.9:73905991::TATATATATATATATATG 869/28218) Row 100777659 (NC_000014.9:73905991::TATATATATATATATATATG 584/28218) Row 100777660 (NC_000014.9:73905991::TATATATATATATATG 289/28218)...	-	Oct 16, 2022 (156)
63	14KJPN Submission ignored due to conflicting rows: Row 100777658 (NC_000014.9:73905991::TATATATATATATATATG 869/28218) Row 100777659 (NC_000014.9:73905991::TATATATATATATATATATG 584/28218) Row 100777660 (NC_000014.9:73905991::TATATATATATATATG 289/28218)...	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 100777658 (NC_000014.9:73905991::TATATATATATATATATG 869/28218) Row 100777659 (NC_000014.9:73905991::TATATATATATATATATATG 584/28218) Row 100777660 (NC_000014.9:73905991::TATATATATATATATG 289/28218)...	-	Oct 16, 2022 (156)
65	ALFA	NC_000014.9 - 73905992	Apr 26, 2021 (155)

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

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4280726169	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATATATGTATA	(self)
ss4280726170	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATATGTATA	(self)
ss4280726171	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATATGTATA	(self)
ss4280726172	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATATATGTATA	(self)
ss4280726173	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATATGTATA	(self)
ss5213933162	NC_000014.8:74372694::TATATATATATA… NC_000014.8:74372694::TATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATGTATA	(self)
ss4280726174, ss5766940558	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATGTATA	(self)
ss4280726175	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATATGTG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATATGTGTATA	(self)
ss3012454781, ss5213933161	NC_000014.8:74372694::TATATATATATA… NC_000014.8:74372694::TATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATGTATA	(self)
ss4280726176, ss5296765809, ss5766940557	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATATGTATA	(self)
13804317, ss3012454778, ss3740519452, ss5213933159	NC_000014.8:74372694::TATATATATATA… NC_000014.8:74372694::TATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATGTATA	(self)
ss4280726177, ss5766940555	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATATGTATA	(self)
ss3012454777, ss5213933158	NC_000014.8:74372694::TATATATATATA… NC_000014.8:74372694::TATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATGTATA	(self)
ss4280726178, ss5296765808, ss5766940554	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATATGTATA	(self)
ss3012454779, ss5213933160	NC_000014.8:74372694::TATATATATATA… NC_000014.8:74372694::TATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATGTATA	(self)
ss4280726179, ss5490756880, ss5766940556	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATATGTATA	(self)
ss4280726180, ss5490756879	NC_000014.9:73905991::TATATATATATA… NC_000014.9:73905991::TATATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATATGTATA	(self)
ss4280726181	NC_000014.9:73905991::TATATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATATGTATA	(self)
ss4280726182	NC_000014.9:73905991::TATATATATG	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATGTATA	NC_000014.9:73905991:TATA:TATATATA… NC_000014.9:73905991:TATA:TATATATATGTATA	(self)
ss4280726183	NC_000014.9:73905991::TATATATG	NC_000014.9:73905991:TATA:TATATATG… NC_000014.9:73905991:TATA:TATATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATATG… NC_000014.9:73905991:TATA:TATATATGTATA	NC_000014.9:73905991:TATA:TATATATG… NC_000014.9:73905991:TATA:TATATATGTATA	(self)
ss4280726184	NC_000014.9:73905991::TATATATGTATA… NC_000014.9:73905991::TATATATGTATATATATATG	NC_000014.9:73905991:TATA:TATATATG… NC_000014.9:73905991:TATA:TATATATGTATATATATATGTATA	(self)
ss4280726185	NC_000014.9:73905991::TATATG	NC_000014.9:73905991:TATA:TATATGTA… NC_000014.9:73905991:TATA:TATATGTATA	(self)
117512492	NC_000014.9:73905991:TATA:TATATGTA… NC_000014.9:73905991:TATA:TATATGTATA	NC_000014.9:73905991:TATA:TATATGTA… NC_000014.9:73905991:TATA:TATATGTATA	(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 rs1491231212

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491231212