SNP Links for Nucleotide (Select 574289185) - SNP

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Select item 14915696161.

rs1491569616 has merged into rs71265963 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTGTGTGTGTG>-,TG,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: 8:72025121 (GRCh38)
8:72937356 (GRCh37)
Canonical SPDI:: NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72025105:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGTGTGTGTGTGTG=0./0 (ALFA)
-=0.17/655 (ALSPAC)
HGVS:: NC_000008.11:g.72025107TG[7], NC_000008.11:g.72025107TG[8], NC_000008.11:g.72025107TG[9], NC_000008.11:g.72025107TG[10], NC_000008.11:g.72025107TG[11], NC_000008.11:g.72025107TG[12], NC_000008.11:g.72025107TG[13], NC_000008.11:g.72025107TG[14], NC_000008.11:g.72025107TG[16], NC_000008.11:g.72025107TG[17], NC_000008.11:g.72025107TG[18], NC_000008.11:g.72025107TG[19], NC_000008.10:g.72937342TG[7], NC_000008.10:g.72937342TG[8], NC_000008.10:g.72937342TG[9], NC_000008.10:g.72937342TG[10], NC_000008.10:g.72937342TG[11], NC_000008.10:g.72937342TG[12], NC_000008.10:g.72937342TG[13], NC_000008.10:g.72937342TG[14], NC_000008.10:g.72937342TG[16], NC_000008.10:g.72937342TG[17], NC_000008.10:g.72937342TG[18], NC_000008.10:g.72937342TG[19], NG_033890.1:g.55450AC[7], NG_033890.1:g.55450AC[8], NG_033890.1:g.55450AC[9], NG_033890.1:g.55450AC[10], NG_033890.1:g.55450AC[11], NG_033890.1:g.55450AC[12], NG_033890.1:g.55450AC[13], NG_033890.1:g.55450AC[14], NG_033890.1:g.55450AC[16], NG_033890.1:g.55450AC[17], NG_033890.1:g.55450AC[18], NG_033890.1:g.55450AC[19]

Select item 14915573012.

rs1491557301 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTT [Show Flanks]
Chromosome:: 8:72049937 (GRCh38)
8:72962173 (GRCh37)
Canonical SPDI:: NC_000008.11:72049937:TTT:TTTATTT
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTATTT=0./0 (ALFA)
TTTA=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72049940_72049941insATTT, NC_000008.10:g.72962175_72962176insATTT, NG_033890.1:g.30647_30648insTAAA

Select item 14915471713.

rs1491547171 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 8:72077289 (GRCh38)
8:72989525 (GRCh37)
Canonical SPDI:: NC_000008.11:72077289:T:TT
Gene:: TRPA1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.00002/1 (GnomAD)
HGVS:: NC_000008.11:g.72077290dup, NC_000008.10:g.72989525dup, NG_033890.1:g.3295dup

Select item 14915377854.

rs1491537785 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGAG,TGAGAGAG,TGATAGAG,TGTGAG,TGTGAGAG,TGTGAGATAGAG,TGTGTGAG,TGTGTGTGAGAGAGAG,TGTGTGTGTGTGAG,TGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGAGAGAGAGAG,TGTGTGTGTGTGTGATAG,TGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGATAGAGAGAG,TGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGTGAGAGAGAGAG,TGTGTGTGTGTGTGTGAGAGAGAGAGAG,TGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGATAGAGAGAG,TGTGTGTGTGTGTGTGATAGATAG,TGTGTGTGTGTGTGTGATAGATAGAG,TGTGTGTGTGTGTGTGATAGATAGAGAGAG,TGTGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGTGTGATAG,TGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGATAGAGAG,TGTGTGTGTGTGTGTGTGATAGATAG,TGTGTGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGAGAGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGTGATAGAGAG,TGTGTGTGTGTGTGTGTGTGATAGAGAGAG,TGTGTGTGTGTGTGTGTGTGATAGATAG,TGTGTGTGTGTGTGTGTGTGATAGATAGAG,TGTGTGTGTGTGTGTGTGTGATAGATAGAGAG,TGTGTGTGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGATAG,TGTGTGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGTGTGATAGAGAG,TGTGTGTGTGTGTGTGTGTGTGATAGATAG,TGTGTGTGTGTGTGTGTGTGTGATAGATAGAG,TGTGTGTGTGTGTGTGTGTGTGATAGATAGAGAG,TGTGTGTGTGTGTGTGTGTGTGGG,TGTGTGTGTGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGATAG,TGTGTGTGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGTGTGTGATAGATAG,TGTGTGTGTGTGTGTGTGTGTGTGATAGATAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGATAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGATAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATAG [Show Flanks]
Chromosome:: 8:72052994 (GRCh38)
8:72965230 (GRCh37)
Canonical SPDI:: NC_000008.11:72052994:G:GTGAG,NC_000008.11:72052994:G:GTGAGAGAG,NC_000008.11:72052994:G:GTGATAGAG,NC_000008.11:72052994:G:GTGTGAG,NC_000008.11:72052994:G:GTGTGAGAG,NC_000008.11:72052994:G:GTGTGAGATAGAG,NC_000008.11:72052994:G:GTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGATAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGAGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGATAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGATAGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGATAGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGATAGATAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGATAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGATAGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGAGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGATAGATAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGATAGATAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGGG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGAGAGAGAGAGAGAGAGAGAGAGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGATAGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGATAGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGATAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGATAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGAGAG,NC_000008.11:72052994:G:GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATAG
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTGAGATAGAG=0./0 (ALFA)
HGVS:: NC_000008.11:g.72052995_72052996insTGAG, NC_000008.11:g.72052995_72052996insTGAGAGAG, NC_000008.11:g.72052995_72052996insTGATAGAG, NC_000008.11:g.72052995GT[2]GAG[1], NC_000008.11:g.72052995GT[2]GA[2]G[1], NC_000008.11:g.72052995GT[2]GA[2]TAGAG[1], NC_000008.11:g.72052995GT[3]GAG[1], NC_000008.11:g.72052995GT[4]GA[4]G[1], NC_000008.11:g.72052995GT[6]GAG[1], NC_000008.11:g.72052995GT[6]GA[4]G[1], NC_000008.11:g.72052995GT[6]GATAGAG[1], NC_000008.11:g.72052995GT[7]GAG[1], NC_000008.11:g.72052995GT[7]GA[2]G[1], NC_000008.11:g.72052995GT[7]GA[3]G[1], NC_000008.11:g.72052995GT[7]GA[4]G[1], NC_000008.11:g.72052995GT[7]GA[5]G[1], NC_000008.11:g.72052995GT[7]GATAG[1], NC_000008.11:g.72052995GT[7]GATAGAG[1], NC_000008.11:g.72052995GT[7]GATAGAGAGAG[1], NC_000008.11:g.72052995GT[8]GAG[1], NC_000008.11:g.72052995GT[8]GA[3]G[1], NC_000008.11:g.72052995GT[8]GA[4]G[1], NC_000008.11:g.72052995GT[8]GA[5]G[1], NC_000008.11:g.72052995GT[8]GA[6]G[1], NC_000008.11:g.72052995GT[8]GATAGAG[1], NC_000008.11:g.72052995GT[8]GATAGAGAGAG[1], NC_000008.11:g.72052995GT[8]GATA[2]G[1], NC_000008.11:g.72052995GT[8]GATA[2]GAG[1], NC_000008.11:g.72052995GT[8]GATA[2]GA[3]G[1], NC_000008.11:g.72052995GT[9]GAG[1], NC_000008.11:g.72052995GT[9]GA[2]G[1], NC_000008.11:g.72052995GT[9]GA[3]G[1], NC_000008.11:g.72052995GT[9]GA[4]G[1], NC_000008.11:g.72052995GT[9]GATAG[1], NC_000008.11:g.72052995GT[9]GATAGAG[1], NC_000008.11:g.72052995GT[9]GATAGAGAG[1], NC_000008.11:g.72052995GT[9]GATA[2]G[1], NC_000008.11:g.72052995GT[10]GAG[1], NC_000008.11:g.72052995GT[10]GA[2]G[1], NC_000008.11:g.72052995GT[10]GA[3]G[1], NC_000008.11:g.72052995GT[10]GA[4]G[1], NC_000008.11:g.72052995GT[10]GA[5]G[1], NC_000008.11:g.72052995GT[10]GA[6]G[1], NC_000008.11:g.72052995GT[10]GATAGAG[1], NC_000008.11:g.72052995GT[10]GATAGAGAG[1], NC_000008.11:g.72052995GT[10]GATAGAGAGAG[1], NC_000008.11:g.72052995GT[10]GATA[2]G[1], NC_000008.11:g.72052995GT[10]GATA[2]GAG[1], NC_000008.11:g.72052995GT[10]GATA[2]GA[2]G[1], NC_000008.11:g.72052995GT[11]GAG[1], NC_000008.11:g.72052995GT[11]GA[2]G[1], NC_000008.11:g.72052995GT[11]GA[3]G[1], NC_000008.11:g.72052995GT[11]GA[4]G[1], NC_000008.11:g.72052995GT[11]GA[5]G[1], NC_000008.11:g.72052995GT[11]GATAG[1], NC_000008.11:g.72052995GT[11]GATAGAG[1], NC_000008.11:g.72052995GT[11]GATAGAGAG[1], NC_000008.11:g.72052995GT[11]GATA[2]G[1], NC_000008.11:g.72052995GT[11]GATA[2]GAG[1], NC_000008.11:g.72052995GT[11]GATA[2]GA[2]G[1], NC_000008.11:g.72052995GT[11]GGG[1], NC_000008.11:g.72052995GT[12]GAG[1], NC_000008.11:g.72052995GT[12]GA[2]G[1], NC_000008.11:g.72052995GT[12]GA[3]G[1], NC_000008.11:g.72052995GT[12]GA[4]G[1], NC_000008.11:g.72052995GT[12]GA[5]G[1], NC_000008.11:g.72052995GT[12]GA[14]G[1], NC_000008.11:g.72052995GT[12]GATAG[1], NC_000008.11:g.72052995GT[12]GATAGAG[1], NC_000008.11:g.72052995GT[12]GATA[2]G[1], NC_000008.11:g.72052995GT[12]GATA[2]GAG[1], NC_000008.11:g.72052995GT[13]GAG[1], NC_000008.11:g.72052995GT[13]GA[2]G[1], NC_000008.11:g.72052995GT[13]GA[3]G[1], NC_000008.11:g.72052995GT[13]GATAGAG[1], NC_000008.11:g.72052995GT[14]GA[3]G[1], NC_000008.11:g.72052995GT[14]GATAG[1], NC_000008.11:g.72052995GT[14]GATAGAG[1], NC_000008.11:g.72052995GT[15]GA[2]G[1], NC_000008.11:g.72052995GT[15]GGGAGAGAG[1], NC_000008.11:g.72052995GT[16]GA[3]G[1], NC_000008.11:g.72052995GT[16]GATAG[1], NC_000008.10:g.72965230_72965231insTGAG, NC_000008.10:g.72965230_72965231insTGAGAGAG, NC_000008.10:g.72965230_72965231insTGATAGAG, NC_000008.10:g.72965230GT[2]GAG[1], NC_000008.10:g.72965230GT[2]GA[2]G[1], NC_000008.10:g.72965230GT[2]GA[2]TAGAG[1], NC_000008.10:g.72965230GT[3]GAG[1], NC_000008.10:g.72965230GT[4]GA[4]G[1], NC_000008.10:g.72965230GT[6]GAG[1], NC_000008.10:g.72965230GT[6]GA[4]G[1], NC_000008.10:g.72965230GT[6]GATAGAG[1], NC_000008.10:g.72965230GT[7]GAG[1], NC_000008.10:g.72965230GT[7]GA[2]G[1], NC_000008.10:g.72965230GT[7]GA[3]G[1], NC_000008.10:g.72965230GT[7]GA[4]G[1], NC_000008.10:g.72965230GT[7]GA[5]G[1], NC_000008.10:g.72965230GT[7]GATAG[1], NC_000008.10:g.72965230GT[7]GATAGAG[1], NC_000008.10:g.72965230GT[7]GATAGAGAGAG[1], NC_000008.10:g.72965230GT[8]GAG[1], NC_000008.10:g.72965230GT[8]GA[3]G[1], NC_000008.10:g.72965230GT[8]GA[4]G[1], NC_000008.10:g.72965230GT[8]GA[5]G[1], NC_000008.10:g.72965230GT[8]GA[6]G[1], NC_000008.10:g.72965230GT[8]GATAGAG[1], NC_000008.10:g.72965230GT[8]GATAGAGAGAG[1], NC_000008.10:g.72965230GT[8]GATA[2]G[1], NC_000008.10:g.72965230GT[8]GATA[2]GAG[1], NC_000008.10:g.72965230GT[8]GATA[2]GA[3]G[1], NC_000008.10:g.72965230GT[9]GAG[1], NC_000008.10:g.72965230GT[9]GA[2]G[1], NC_000008.10:g.72965230GT[9]GA[3]G[1], NC_000008.10:g.72965230GT[9]GA[4]G[1], NC_000008.10:g.72965230GT[9]GATAG[1], NC_000008.10:g.72965230GT[9]GATAGAG[1], NC_000008.10:g.72965230GT[9]GATAGAGAG[1], NC_000008.10:g.72965230GT[9]GATA[2]G[1], NC_000008.10:g.72965230GT[10]GAG[1], NC_000008.10:g.72965230GT[10]GA[2]G[1], NC_000008.10:g.72965230GT[10]GA[3]G[1], NC_000008.10:g.72965230GT[10]GA[4]G[1], NC_000008.10:g.72965230GT[10]GA[5]G[1], NC_000008.10:g.72965230GT[10]GA[6]G[1], NC_000008.10:g.72965230GT[10]GATAGAG[1], NC_000008.10:g.72965230GT[10]GATAGAGAG[1], NC_000008.10:g.72965230GT[10]GATAGAGAGAG[1], NC_000008.10:g.72965230GT[10]GATA[2]G[1], NC_000008.10:g.72965230GT[10]GATA[2]GAG[1], NC_000008.10:g.72965230GT[10]GATA[2]GA[2]G[1], NC_000008.10:g.72965230GT[11]GAG[1], NC_000008.10:g.72965230GT[11]GA[2]G[1], NC_000008.10:g.72965230GT[11]GA[3]G[1], NC_000008.10:g.72965230GT[11]GA[4]G[1], NC_000008.10:g.72965230GT[11]GA[5]G[1], NC_000008.10:g.72965230GT[11]GATAG[1], NC_000008.10:g.72965230GT[11]GATAGAG[1], NC_000008.10:g.72965230GT[11]GATAGAGAG[1], NC_000008.10:g.72965230GT[11]GATA[2]G[1], NC_000008.10:g.72965230GT[11]GATA[2]GAG[1], NC_000008.10:g.72965230GT[11]GATA[2]GA[2]G[1], NC_000008.10:g.72965230GT[11]GGG[1], NC_000008.10:g.72965230GT[12]GAG[1], NC_000008.10:g.72965230GT[12]GA[2]G[1], NC_000008.10:g.72965230GT[12]GA[3]G[1], NC_000008.10:g.72965230GT[12]GA[4]G[1], NC_000008.10:g.72965230GT[12]GA[5]G[1], NC_000008.10:g.72965230GT[12]GA[14]G[1], NC_000008.10:g.72965230GT[12]GATAG[1], NC_000008.10:g.72965230GT[12]GATAGAG[1], NC_000008.10:g.72965230GT[12]GATA[2]G[1], NC_000008.10:g.72965230GT[12]GATA[2]GAG[1], NC_000008.10:g.72965230GT[13]GAG[1], NC_000008.10:g.72965230GT[13]GA[2]G[1], NC_000008.10:g.72965230GT[13]GA[3]G[1], NC_000008.10:g.72965230GT[13]GATAGAG[1], NC_000008.10:g.72965230GT[14]GA[3]G[1], NC_000008.10:g.72965230GT[14]GATAG[1], NC_000008.10:g.72965230GT[14]GATAGAG[1], NC_000008.10:g.72965230GT[15]GA[2]G[1], NC_000008.10:g.72965230GT[15]GGGAGAGAG[1], NC_000008.10:g.72965230GT[16]GA[3]G[1], NC_000008.10:g.72965230GT[16]GATAG[1], NG_033890.1:g.27590_27591insTCAC, NG_033890.1:g.27590CT[3]CAC[1], NG_033890.1:g.27590CT[2]ATCAC[1], NG_033890.1:g.27590_27591insTCACAC, NG_033890.1:g.27590CT[2]CA[2]C[1], NG_033890.1:g.27590CT[2]ATCTCACAC[1], NG_033890.1:g.27590_27591insTCACACAC, NG_033890.1:g.27590CT[4]CA[4]C[1], NG_033890.1:g.27590_27591insTCACACACACACAC, NG_033890.1:g.27590CT[4]CA[6]C[1], NG_033890.1:g.27590CT[2]ATCACACACACACAC[1], NG_033890.1:g.27590_27591insTCACACACACACACAC, NG_033890.1:g.27590CT[2]CA[7]C[1], NG_033890.1:g.27590CT[3]CA[7]C[1], NG_033890.1:g.27590CT[4]CA[7]C[1], NG_033890.1:g.27590CT[5]CA[7]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACAC, NG_033890.1:g.27590CT[2]ATCACACACACACACAC[1], NG_033890.1:g.27590CT[4]ATCACACACACACACAC[1], NG_033890.1:g.27590_27591insTCACACACACACACACAC, NG_033890.1:g.27590CT[3]CA[8]C[1], NG_033890.1:g.27590CT[4]CA[8]C[1], NG_033890.1:g.27590CT[5]CA[8]C[1], NG_033890.1:g.27590CT[6]CA[8]C[1], NG_033890.1:g.27590CT[2]ATCACACACACACACACAC[1], NG_033890.1:g.27590CT[4]ATCACACACACACACACAC[1], NG_033890.1:g.27590CTAT[2]CA[8]C[1], NG_033890.1:g.27590CT[2]ATCTATCACACACACACACACAC[1], NG_033890.1:g.27590CT[4]ATCTATCACACACACACACACAC[1], NG_033890.1:g.27590_27591insTCACACACACACACACACAC, NG_033890.1:g.27590CT[2]CA[9]C[1], NG_033890.1:g.27590CT[3]CA[9]C[1], NG_033890.1:g.27590CT[4]CA[9]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACACACAC, NG_033890.1:g.27590CT[2]ATCACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]ATCACACACACACACACACAC[1], NG_033890.1:g.27590CTAT[2]CA[9]C[1], NG_033890.1:g.27590_27591insTCACACACACACACACACACAC, NG_033890.1:g.27590CT[2]CA[10]C[1], NG_033890.1:g.27590CT[3]CA[10]C[1], NG_033890.1:g.27590CT[4]CA[10]C[1], NG_033890.1:g.27590CT[5]CA[10]C[1], NG_033890.1:g.27590CT[6]CA[10]C[1], NG_033890.1:g.27590CT[2]ATCACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]ATCACACACACACACACACACAC[1], NG_033890.1:g.27590CT[4]ATCACACACACACACACACACAC[1], NG_033890.1:g.27590CTAT[2]CA[10]C[1], NG_033890.1:g.27590CT[2]ATCTATCACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]ATCTATCACACACACACACACACACAC[1], NG_033890.1:g.27590_27591insTCACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]CA[11]C[1], NG_033890.1:g.27590CT[3]CA[11]C[1], NG_033890.1:g.27590CT[4]CA[11]C[1], NG_033890.1:g.27590CT[5]CA[11]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]ATCACACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]ATCACACACACACACACACACACAC[1], NG_033890.1:g.27590CTAT[2]CA[11]C[1], NG_033890.1:g.27590CT[2]ATCTATCACACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]ATCTATCACACACACACACACACACACAC[1], NG_033890.1:g.27590_27591insCCACACACACACACACACACACAC, NG_033890.1:g.27590_27591insTCACACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]CA[12]C[1], NG_033890.1:g.27590CT[3]CA[12]C[1], NG_033890.1:g.27590CT[4]CA[12]C[1], NG_033890.1:g.27590CT[5]CA[12]C[1], NG_033890.1:g.27590CT[14]CA[12]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]ATCACACACACACACACACACACACAC[1], NG_033890.1:g.27590CTAT[2]CA[12]C[1], NG_033890.1:g.27590CT[2]ATCTATCACACACACACACACACACACACAC[1], NG_033890.1:g.27590_27591insTCACACACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]CA[13]C[1], NG_033890.1:g.27590CT[3]CA[13]C[1], NG_033890.1:g.27590CT[2]ATCACACACACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]CA[14]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACACACACACACACACAC, NG_033890.1:g.27590CT[2]ATCACACACACACACACACACACACACACAC[1], NG_033890.1:g.27590CT[2]CA[15]C[1], NG_033890.1:g.27590CT[3]CCCACACACACACACACACACACACACACACAC[1], NG_033890.1:g.27590CT[3]CA[16]C[1], NG_033890.1:g.27590_27591insTATCACACACACACACACACACACACACACACACAC, NR_033652.1:n.1485_1486insTGAG, NR_033652.1:n.1485_1486insTGAGAGAG, NR_033652.1:n.1485_1486insTGATAGAG, NR_033652.1:n.1485GT[2]GAG[1], NR_033652.1:n.1485GT[2]GA[2]G[1], NR_033652.1:n.1485GT[2]GA[2]TAGAG[1], NR_033652.1:n.1485GT[3]GAG[1], NR_033652.1:n.1485GT[4]GA[4]G[1], NR_033652.1:n.1485GT[6]GAG[1], NR_033652.1:n.1485GT[6]GA[4]G[1], NR_033652.1:n.1485GT[6]GATAGAG[1], NR_033652.1:n.1485GT[7]GAG[1], NR_033652.1:n.1485GT[7]GA[2]G[1], NR_033652.1:n.1485GT[7]GA[3]G[1], NR_033652.1:n.1485GT[7]GA[4]G[1], NR_033652.1:n.1485GT[7]GA[5]G[1], NR_033652.1:n.1485GT[7]GATAG[1], NR_033652.1:n.1485GT[7]GATAGAG[1], NR_033652.1:n.1485GT[7]GATAGAGAGAG[1], NR_033652.1:n.1485GT[8]GAG[1], NR_033652.1:n.1485GT[8]GA[3]G[1], NR_033652.1:n.1485GT[8]GA[4]G[1], NR_033652.1:n.1485GT[8]GA[5]G[1], NR_033652.1:n.1485GT[8]GA[6]G[1], NR_033652.1:n.1485GT[8]GATAGAG[1], NR_033652.1:n.1485GT[8]GATAGAGAGAG[1], NR_033652.1:n.1485GT[8]GATA[2]G[1], NR_033652.1:n.1485GT[8]GATA[2]GAG[1], NR_033652.1:n.1485GT[8]GATA[2]GA[3]G[1], NR_033652.1:n.1485GT[9]GAG[1], NR_033652.1:n.1485GT[9]GA[2]G[1], NR_033652.1:n.1485GT[9]GA[3]G[1], NR_033652.1:n.1485GT[9]GA[4]G[1], NR_033652.1:n.1485GT[9]GATAG[1], NR_033652.1:n.1485GT[9]GATAGAG[1], NR_033652.1:n.1485GT[9]GATAGAGAG[1], NR_033652.1:n.1485GT[9]GATA[2]G[1], NR_033652.1:n.1485GT[10]GAG[1], NR_033652.1:n.1485GT[10]GA[2]G[1], NR_033652.1:n.1485GT[10]GA[3]G[1], NR_033652.1:n.1485GT[10]GA[4]G[1], NR_033652.1:n.1485GT[10]GA[5]G[1], NR_033652.1:n.1485GT[10]GA[6]G[1], NR_033652.1:n.1485GT[10]GATAGAG[1], NR_033652.1:n.1485GT[10]GATAGAGAG[1], NR_033652.1:n.1485GT[10]GATAGAGAGAG[1], NR_033652.1:n.1485GT[10]GATA[2]G[1], NR_033652.1:n.1485GT[10]GATA[2]GAG[1], NR_033652.1:n.1485GT[10]GATA[2]GA[2]G[1], NR_033652.1:n.1485GT[11]GAG[1], NR_033652.1:n.1485GT[11]GA[2]G[1], NR_033652.1:n.1485GT[11]GA[3]G[1], NR_033652.1:n.1485GT[11]GA[4]G[1], NR_033652.1:n.1485GT[11]GA[5]G[1], NR_033652.1:n.1485GT[11]GATAG[1], NR_033652.1:n.1485GT[11]GATAGAG[1], NR_033652.1:n.1485GT[11]GATAGAGAG[1], NR_033652.1:n.1485GT[11]GATA[2]G[1], NR_033652.1:n.1485GT[11]GATA[2]GAG[1], NR_033652.1:n.1485GT[11]GATA[2]GA[2]G[1], NR_033652.1:n.1485GT[11]GGG[1], NR_033652.1:n.1485GT[12]GAG[1], NR_033652.1:n.1485GT[12]GA[2]G[1], NR_033652.1:n.1485GT[12]GA[3]G[1], NR_033652.1:n.1485GT[12]GA[4]G[1], NR_033652.1:n.1485GT[12]GA[5]G[1], NR_033652.1:n.1485GT[12]GA[14]G[1], NR_033652.1:n.1485GT[12]GATAG[1], NR_033652.1:n.1485GT[12]GATAGAG[1], NR_033652.1:n.1485GT[12]GATA[2]G[1], NR_033652.1:n.1485GT[12]GATA[2]GAG[1], NR_033652.1:n.1485GT[13]GAG[1], NR_033652.1:n.1485GT[13]GA[2]G[1], NR_033652.1:n.1485GT[13]GA[3]G[1], NR_033652.1:n.1485GT[13]GATAGAG[1], NR_033652.1:n.1485GT[14]GA[3]G[1], NR_033652.1:n.1485GT[14]GATAG[1], NR_033652.1:n.1485GT[14]GATAGAG[1], NR_033652.1:n.1485GT[15]GA[2]G[1], NR_033652.1:n.1485GT[15]GGGAGAGAG[1], NR_033652.1:n.1485GT[16]GA[3]G[1], NR_033652.1:n.1485GT[16]GATAG[1], NR_033651.1:n.890_891insTGAG, NR_033651.1:n.890_891insTGAGAGAG, NR_033651.1:n.890_891insTGATAGAG, NR_033651.1:n.890GT[2]GAG[1], NR_033651.1:n.890GT[2]GA[2]G[1], NR_033651.1:n.890GT[2]GA[2]TAGAG[1], NR_033651.1:n.890GT[3]GAG[1], NR_033651.1:n.890GT[4]GA[4]G[1], NR_033651.1:n.890GT[6]GAG[1], NR_033651.1:n.890GT[6]GA[4]G[1], NR_033651.1:n.890GT[6]GATAGAG[1], NR_033651.1:n.890GT[7]GAG[1], NR_033651.1:n.890GT[7]GA[2]G[1], NR_033651.1:n.890GT[7]GA[3]G[1], NR_033651.1:n.890GT[7]GA[4]G[1], NR_033651.1:n.890GT[7]GA[5]G[1], NR_033651.1:n.890GT[7]GATAG[1], NR_033651.1:n.890GT[7]GATAGAG[1], NR_033651.1:n.890GT[7]GATAGAGAGAG[1], NR_033651.1:n.890GT[8]GAG[1], NR_033651.1:n.890GT[8]GA[3]G[1], NR_033651.1:n.890GT[8]GA[4]G[1], NR_033651.1:n.890GT[8]GA[5]G[1], NR_033651.1:n.890GT[8]GA[6]G[1], NR_033651.1:n.890GT[8]GATAGAG[1], NR_033651.1:n.890GT[8]GATAGAGAGAG[1], NR_033651.1:n.890GT[8]GATA[2]G[1], NR_033651.1:n.890GT[8]GATA[2]GAG[1], NR_033651.1:n.890GT[8]GATA[2]GA[3]G[1], NR_033651.1:n.890GT[9]GAG[1], NR_033651.1:n.890GT[9]GA[2]G[1], NR_033651.1:n.890GT[9]GA[3]G[1], NR_033651.1:n.890GT[9]GA[4]G[1], NR_033651.1:n.890GT[9]GATAG[1], NR_033651.1:n.890GT[9]GATAGAG[1], NR_033651.1:n.890GT[9]GATAGAGAG[1], NR_033651.1:n.890GT[9]GATA[2]G[1], NR_033651.1:n.890GT[10]GAG[1], NR_033651.1:n.890GT[10]GA[2]G[1], NR_033651.1:n.890GT[10]GA[3]G[1], NR_033651.1:n.890GT[10]GA[4]G[1], NR_033651.1:n.890GT[10]GA[5]G[1], NR_033651.1:n.890GT[10]GA[6]G[1], NR_033651.1:n.890GT[10]GATAGAG[1], NR_033651.1:n.890GT[10]GATAGAGAG[1], NR_033651.1:n.890GT[10]GATAGAGAGAG[1], NR_033651.1:n.890GT[10]GATA[2]G[1], NR_033651.1:n.890GT[10]GATA[2]GAG[1], NR_033651.1:n.890GT[10]GATA[2]GA[2]G[1], NR_033651.1:n.890GT[11]GAG[1], NR_033651.1:n.890GT[11]GA[2]G[1], NR_033651.1:n.890GT[11]GA[3]G[1], NR_033651.1:n.890GT[11]GA[4]G[1], NR_033651.1:n.890GT[11]GA[5]G[1], NR_033651.1:n.890GT[11]GATAG[1], NR_033651.1:n.890GT[11]GATAGAG[1], NR_033651.1:n.890GT[11]GATAGAGAG[1], NR_033651.1:n.890GT[11]GATA[2]G[1], NR_033651.1:n.890GT[11]GATA[2]GAG[1], NR_033651.1:n.890GT[11]GATA[2]GA[2]G[1], NR_033651.1:n.890GT[11]GGG[1], NR_033651.1:n.890GT[12]GAG[1], NR_033651.1:n.890GT[12]GA[2]G[1], NR_033651.1:n.890GT[12]GA[3]G[1], NR_033651.1:n.890GT[12]GA[4]G[1], NR_033651.1:n.890GT[12]GA[5]G[1], NR_033651.1:n.890GT[12]GA[14]G[1], NR_033651.1:n.890GT[12]GATAG[1], NR_033651.1:n.890GT[12]GATAGAG[1], NR_033651.1:n.890GT[12]GATA[2]G[1], NR_033651.1:n.890GT[12]GATA[2]GAG[1], NR_033651.1:n.890GT[13]GAG[1], NR_033651.1:n.890GT[13]GA[2]G[1], NR_033651.1:n.890GT[13]GA[3]G[1], NR_033651.1:n.890GT[13]GATAGAG[1], NR_033651.1:n.890GT[14]GA[3]G[1], NR_033651.1:n.890GT[14]GATAG[1], NR_033651.1:n.890GT[14]GATAGAG[1], NR_033651.1:n.890GT[15]GA[2]G[1], NR_033651.1:n.890GT[15]GGGAGAGAG[1], NR_033651.1:n.890GT[16]GA[3]G[1], NR_033651.1:n.890GT[16]GATAG[1]

Select item 14915293245.

rs1491529324 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGA>-,GA,GAGAGA [Show Flanks]
Chromosome:: 8:72052997 (GRCh38)
8:72965232 (GRCh37)
Canonical SPDI:: NC_000008.11:72052994:GAGAGA:GA,NC_000008.11:72052994:GAGAGA:GAGA,NC_000008.11:72052994:GAGAGA:GAGAGAGA
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGA=0.00154/25 (ALFA)
GA=0.00274/5 (Korea1K)
HGVS:: NC_000008.11:g.72052995GA[1], NC_000008.11:g.72052995GA[2], NC_000008.11:g.72052995GA[4], NC_000008.10:g.72965230GA[1], NC_000008.10:g.72965230GA[2], NC_000008.10:g.72965230GA[4], NG_033890.1:g.27585TC[1], NG_033890.1:g.27585TC[2], NG_033890.1:g.27585TC[4], NR_033652.1:n.1485GA[1], NR_033652.1:n.1485GA[2], NR_033652.1:n.1485GA[4], NR_033651.1:n.890GA[1], NR_033651.1:n.890GA[2], NR_033651.1:n.890GA[4]

Select item 14915013156.

rs1491501315 has merged into rs34558929 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTTTTTTT [Show Flanks]
Chromosome:: 8:72060873 (GRCh38)
8:72973108 (GRCh37)
Canonical SPDI:: NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:72060860:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: TRPA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.16722/100 (NorthernSweden)
-=0.24754/954 (ALSPAC)
-=0.25/10 (GENOME_DK)
-=0.26348/977 (TWINSUK)
-=0.33646/1685 (1000Genomes)
HGVS:: NC_000008.11:g.72060873_72060874del, NC_000008.11:g.72060874del, NC_000008.11:g.72060874dup, NC_000008.11:g.72060873_72060874dup, NC_000008.11:g.72060872_72060874dup, NC_000008.11:g.72060866_72060874dup, NC_000008.10:g.72973108_72973109del, NC_000008.10:g.72973109del, NC_000008.10:g.72973109dup, NC_000008.10:g.72973108_72973109dup, NC_000008.10:g.72973107_72973109dup, NC_000008.10:g.72973101_72973109dup, NG_033890.1:g.19723_19724del, NG_033890.1:g.19724del, NG_033890.1:g.19724dup, NG_033890.1:g.19723_19724dup, NG_033890.1:g.19722_19724dup, NG_033890.1:g.19716_19724dup

Select item 14914808127.

rs1491480812 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,G [Show Flanks]
Chromosome:: 8:72053006 (GRCh38)
8:72965242 (GRCh37)
Canonical SPDI:: NC_000008.11:72053006::C,NC_000008.11:72053006::G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.00233/187 (GnomAD)
HGVS:: NC_000008.11:g.72053006_72053007insC, NC_000008.11:g.72053006_72053007insG, NC_000008.10:g.72965241_72965242insC, NC_000008.10:g.72965241_72965242insG, NG_033890.1:g.27578_27579insG, NG_033890.1:g.27578_27579insC, NR_033652.1:n.1496_1497insC, NR_033652.1:n.1496_1497insG, NR_033651.1:n.901_902insC, NR_033651.1:n.901_902insG

Select item 14914117878.

rs1491411787 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGCTATAGTTTCT [Show Flanks]
Chromosome:: 8:72060861 (GRCh38)
8:72973097 (GRCh37)
Canonical SPDI:: NC_000008.11:72060861:T:TAGCTATAGTTTCT
Gene:: TRPA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TAGCTATAGTTTCT=0./0 (ALFA)
HGVS:: NC_000008.11:g.72060862_72060863insAGCTATAGTTTCT, NC_000008.10:g.72973097_72973098insAGCTATAGTTTCT, NG_033890.1:g.19723_19724insGAAACTATAGCTA

Select item 14912983259.

rs1491298325 has merged into rs111426953 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT [Show Flanks]
Chromosome:: 8:72049945 (GRCh38)
8:72962180 (GRCh37)
Canonical SPDI:: NC_000008.11:72049936:TTTTTTTTTTT:TTTTTTTT,NC_000008.11:72049936:TTTTTTTTTTT:TTTTTTTTT,NC_000008.11:72049936:TTTTTTTTTTT:TTTTTTTTTT,NC_000008.11:72049936:TTTTTTTTTTT:TTTTTTTTTTTT
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
T=0.45/18 (GENOME_DK)
T=0.467645/123781 (TOPMED)
-=0.47/282 (NorthernSweden)
-=0.496994/496 (GoNL)
T=0.498962/1923 (ALSPAC)
T=0.499461/1852 (TWINSUK)
HGVS:: NC_000008.11:g.72049945_72049947del, NC_000008.11:g.72049946_72049947del, NC_000008.11:g.72049947del, NC_000008.11:g.72049947dup, NC_000008.10:g.72962180_72962182del, NC_000008.10:g.72962181_72962182del, NC_000008.10:g.72962182del, NC_000008.10:g.72962182dup, NG_033890.1:g.30646_30648del, NG_033890.1:g.30647_30648del, NG_033890.1:g.30648del, NG_033890.1:g.30648dup

Select item 149118034310.

rs1491180343 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 8:72077290 (GRCh38)
8:72989525 (GRCh37)
Canonical SPDI:: NC_000008.11:72077288:GTG:G
Gene:: TRPA1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.01627/193 (ALFA)
-=0.0039/110 (TOMMO)
HGVS:: NC_000008.11:g.72077290_72077291del, NC_000008.10:g.72989525_72989526del, NG_033890.1:g.3295_3296del

Select item 149102828411.

rs1491028284 has merged into rs34929058 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: 8:72063394 (GRCh38)
8:72975629 (GRCh37)
Canonical SPDI:: NC_000008.11:72063384:AAAAAAAAAAA:AAAAAAAAA,NC_000008.11:72063384:AAAAAAAAAAA:AAAAAAAAAA,NC_000008.11:72063384:AAAAAAAAAAA:AAAAAAAAAAAA
Gene:: TRPA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0.00017/1 (ALFA)
A=0.02091/351 (TOMMO)
A=0.02456/45 (Korea1K)
A=0.21224/1061 (1000Genomes)
A=0.325/13 (GENOME_DK)
A=0.39914/1480 (TWINSUK)
A=0.40322/1554 (ALSPAC)
A=0.42333/254 (NorthernSweden)
HGVS:: NC_000008.11:g.72063394_72063395del, NC_000008.11:g.72063395del, NC_000008.11:g.72063395dup, NC_000008.10:g.72975629_72975630del, NC_000008.10:g.72975630del, NC_000008.10:g.72975630dup, NG_033890.1:g.17199_17200del, NG_033890.1:g.17200del, NG_033890.1:g.17200dup

Select item 149093411912.

rs1490934119 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 8:72075894 (GRCh38)
8:72988129 (GRCh37)
Canonical SPDI:: NC_000008.11:72075893:G:
Gene:: TRPA1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.00141/24 (TOMMO)
HGVS:: NC_000008.11:g.72075894del, NC_000008.10:g.72988129del, NG_033890.1:g.4691del

Select item 149087224213.

rs1490872242 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:72021058 (GRCh38)
8:72933293 (GRCh37)
Canonical SPDI:: NC_000008.11:72021057:G:T
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000008.11:g.72021058G>T, NC_000008.10:g.72933293G>T, NG_033890.1:g.59527C>A

Select item 149085921714.

rs1490859217 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:72036784 (GRCh38)
8:72949019 (GRCh37)
Canonical SPDI:: NC_000008.11:72036783:T:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.72036784T>G, NC_000008.10:g.72949019T>G, NG_033890.1:g.43801A>C

Select item 149084606315.

rs1490846063 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:72022134 (GRCh38)
8:72934369 (GRCh37)
Canonical SPDI:: NC_000008.11:72022133:G:C
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72022134G>C, NC_000008.10:g.72934369G>C, NG_033890.1:g.58451C>G, NM_007332.3:c.*772C>G, NM_007332.2:c.*772C>G, XM_011517625.3:c.*772C>G, XM_011517625.2:c.*772C>G, XM_011517625.1:c.*772C>G, XM_011517624.3:c.*772C>G, XM_011517624.2:c.*772C>G, XM_011517624.1:c.*772C>G

Select item 149081235816.

rs1490812358 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:72026031 (GRCh38)
8:72938266 (GRCh37)
Canonical SPDI:: NC_000008.11:72026030:A:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.72026031A>G, NC_000008.10:g.72938266A>G, NG_033890.1:g.54554T>C, NM_007332.3:c.2980T>C, NM_007332.2:c.2980T>C, XM_011517625.3:c.2980T>C, XM_011517625.2:c.2980T>C, XM_011517625.1:c.2980T>C, XM_011517624.3:c.3055T>C, XM_011517624.2:c.3055T>C, XM_011517624.1:c.3055T>C, NP_015628.2:p.Phe994Leu, XP_011515927.1:p.Phe994Leu, XP_011515926.1:p.Phe1019Leu

Select item 149079096217.

rs1490790962 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:72030502 (GRCh38)
8:72942737 (GRCh37)
Canonical SPDI:: NC_000008.11:72030501:A:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.72030502A>G, NC_000008.10:g.72942737A>G, NG_033890.1:g.50083T>C

Select item 149076630618.

rs1490766306 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:72029385 (GRCh38)
8:72941620 (GRCh37)
Canonical SPDI:: NC_000008.11:72029384:C:T
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72029385C>T, NC_000008.10:g.72941620C>T, NG_033890.1:g.51200G>A

Select item 149072394819.

rs1490723948 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:72071267 (GRCh38)
8:72983502 (GRCh37)
Canonical SPDI:: NC_000008.11:72071266:C:A,NC_000008.11:72071266:C:G,NC_000008.11:72071266:C:T
Gene:: TRPA1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
A=0.000106/2 (TOMMO)
HGVS:: NC_000008.11:g.72071267C>A, NC_000008.11:g.72071267C>G, NC_000008.11:g.72071267C>T, NC_000008.10:g.72983502C>A, NC_000008.10:g.72983502C>G, NC_000008.10:g.72983502C>T, NG_033890.1:g.9318G>T, NG_033890.1:g.9318G>C, NG_033890.1:g.9318G>A

Select item 149067841920.

rs1490678419 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:72020026 (GRCh38)
8:72932261 (GRCh37)
Canonical SPDI:: NC_000008.11:72020025:G:T
Gene:: MSC-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.72020026G>T, NC_000008.10:g.72932261G>T, NG_033890.1:g.60559C>A

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