SNP Links for Nucleotide (Select 295849284) - SNP

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Select item 14915377851.

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 14915293242.

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 14914808123.

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 14904323404.

rs1490432340 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:72054620 (GRCh38)
8:72966855 (GRCh37)
Canonical SPDI:: NC_000008.11:72054619:C:T
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.72054620C>T, NC_000008.10:g.72966855C>T, NG_033890.1:g.25965G>A, NR_033652.1:n.3110C>T, NR_033651.1:n.2515C>T

Select item 14899439695.

rs1489943969 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:72055075 (GRCh38)
8:72967310 (GRCh37)
Canonical SPDI:: NC_000008.11:72055074:C:A,NC_000008.11:72055074:C:T
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72055075C>A, NC_000008.11:g.72055075C>T, NC_000008.10:g.72967310C>A, NC_000008.10:g.72967310C>T, NG_033890.1:g.25510G>T, NG_033890.1:g.25510G>A, NR_033652.1:n.3565C>A, NR_033652.1:n.3565C>T, NR_033651.1:n.2970C>A, NR_033651.1:n.2970C>T

Select item 14895187316.

rs1489518731 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:72053410 (GRCh38)
8:72965645 (GRCh37)
Canonical SPDI:: NC_000008.11:72053409:A:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000036/5 (GnomAD)
HGVS:: NC_000008.11:g.72053410A>G, NC_000008.10:g.72965645A>G, NG_033890.1:g.27175T>C, NR_033652.1:n.1900A>G, NR_033651.1:n.1305A>G

Select item 14890413657.

rs1489041365 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:72053046 (GRCh38)
8:72965281 (GRCh37)
Canonical SPDI:: NC_000008.11:72053045:T:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00157/7 (ALFA)
A=0.00106/18 (TOMMO)
A=0.00125/8 (1000Genomes)
A=0.00156/7 (Estonian)
HGVS:: NC_000008.11:g.72053046T>A, NC_000008.10:g.72965281T>A, NG_033890.1:g.27539A>T, NR_033652.1:n.1536T>A, NR_033651.1:n.941T>A

Select item 14885159238.

rs1488515923 has merged into rs57129422 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTGTGTGTGTG>-,TGTG,TGTGTG,TGTGTGTG,TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
Chromosome:: 8:72052980 (GRCh38)
8:72965215 (GRCh37)
Canonical SPDI:: NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000008.11:72052965:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGTG=0./0 (ALFA)
HGVS:: NC_000008.11:g.72052966TG[7], NC_000008.11:g.72052966TG[9], NC_000008.11:g.72052966TG[10], NC_000008.11:g.72052966TG[11], NC_000008.11:g.72052966TG[12], NC_000008.11:g.72052966TG[13], NC_000008.11:g.72052966TG[14], NC_000008.11:g.72052966TG[16], NC_000008.11:g.72052966TG[17], NC_000008.11:g.72052966TG[18], NC_000008.11:g.72052966TG[19], NC_000008.11:g.72052966TG[20], NC_000008.11:g.72052966TG[21], NC_000008.11:g.72052966TG[22], NC_000008.11:g.72052966TG[23], NC_000008.11:g.72052966TG[24], NC_000008.11:g.72052966TG[25], NC_000008.11:g.72052966TG[26], NC_000008.11:g.72052966TG[27], NC_000008.11:g.72052966TG[28], NC_000008.11:g.72052966TG[29], NC_000008.11:g.72052966TG[30], NC_000008.11:g.72052966TG[31], NC_000008.11:g.72052966TG[32], NC_000008.11:g.72052966TG[33], NC_000008.10:g.72965201TG[7], NC_000008.10:g.72965201TG[9], NC_000008.10:g.72965201TG[10], NC_000008.10:g.72965201TG[11], NC_000008.10:g.72965201TG[12], NC_000008.10:g.72965201TG[13], NC_000008.10:g.72965201TG[14], NC_000008.10:g.72965201TG[16], NC_000008.10:g.72965201TG[17], NC_000008.10:g.72965201TG[18], NC_000008.10:g.72965201TG[19], NC_000008.10:g.72965201TG[20], NC_000008.10:g.72965201TG[21], NC_000008.10:g.72965201TG[22], NC_000008.10:g.72965201TG[23], NC_000008.10:g.72965201TG[24], NC_000008.10:g.72965201TG[25], NC_000008.10:g.72965201TG[26], NC_000008.10:g.72965201TG[27], NC_000008.10:g.72965201TG[28], NC_000008.10:g.72965201TG[29], NC_000008.10:g.72965201TG[30], NC_000008.10:g.72965201TG[31], NC_000008.10:g.72965201TG[32], NC_000008.10:g.72965201TG[33], NG_033890.1:g.27590CA[7], NG_033890.1:g.27590CA[9], NG_033890.1:g.27590CA[10], NG_033890.1:g.27590CA[11], NG_033890.1:g.27590CA[12], NG_033890.1:g.27590CA[13], NG_033890.1:g.27590CA[14], NG_033890.1:g.27590CA[16], NG_033890.1:g.27590CA[17], NG_033890.1:g.27590CA[18], NG_033890.1:g.27590CA[19], NG_033890.1:g.27590CA[20], NG_033890.1:g.27590CA[21], NG_033890.1:g.27590CA[22], NG_033890.1:g.27590CA[23], NG_033890.1:g.27590CA[24], NG_033890.1:g.27590CA[25], NG_033890.1:g.27590CA[26], NG_033890.1:g.27590CA[27], NG_033890.1:g.27590CA[28], NG_033890.1:g.27590CA[29], NG_033890.1:g.27590CA[30], NG_033890.1:g.27590CA[31], NG_033890.1:g.27590CA[32], NG_033890.1:g.27590CA[33], NR_033652.1:n.1456TG[7], NR_033652.1:n.1456TG[9], NR_033652.1:n.1456TG[10], NR_033652.1:n.1456TG[11], NR_033652.1:n.1456TG[12], NR_033652.1:n.1456TG[13], NR_033652.1:n.1456TG[14], NR_033652.1:n.1456TG[16], NR_033652.1:n.1456TG[17], NR_033652.1:n.1456TG[18], NR_033652.1:n.1456TG[19], NR_033652.1:n.1456TG[20], NR_033652.1:n.1456TG[21], NR_033652.1:n.1456TG[22], NR_033652.1:n.1456TG[23], NR_033652.1:n.1456TG[24], NR_033652.1:n.1456TG[25], NR_033652.1:n.1456TG[26], NR_033652.1:n.1456TG[27], NR_033652.1:n.1456TG[28], NR_033652.1:n.1456TG[29], NR_033652.1:n.1456TG[30], NR_033652.1:n.1456TG[31], NR_033652.1:n.1456TG[32], NR_033652.1:n.1456TG[33], NR_033651.1:n.861TG[7], NR_033651.1:n.861TG[9], NR_033651.1:n.861TG[10], NR_033651.1:n.861TG[11], NR_033651.1:n.861TG[12], NR_033651.1:n.861TG[13], NR_033651.1:n.861TG[14], NR_033651.1:n.861TG[16], NR_033651.1:n.861TG[17], NR_033651.1:n.861TG[18], NR_033651.1:n.861TG[19], NR_033651.1:n.861TG[20], NR_033651.1:n.861TG[21], NR_033651.1:n.861TG[22], NR_033651.1:n.861TG[23], NR_033651.1:n.861TG[24], NR_033651.1:n.861TG[25], NR_033651.1:n.861TG[26], NR_033651.1:n.861TG[27], NR_033651.1:n.861TG[28], NR_033651.1:n.861TG[29], NR_033651.1:n.861TG[30], NR_033651.1:n.861TG[31], NR_033651.1:n.861TG[32], NR_033651.1:n.861TG[33]

Select item 14878065799.

rs1487806579 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:72054038 (GRCh38)
8:72966273 (GRCh37)
Canonical SPDI:: NC_000008.11:72054037:A:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000008.11:g.72054038A>G, NC_000008.10:g.72966273A>G, NG_033890.1:g.26547T>C, NR_033652.1:n.2528A>G, NR_033651.1:n.1933A>G

Select item 148766427210.

rs1487664272 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:72055510 (GRCh38)
8:72967745 (GRCh37)
Canonical SPDI:: NC_000008.11:72055509:A:C
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.72055510A>C, NC_000008.10:g.72967745A>C, NG_033890.1:g.25075T>G, NM_007332.3:c.1455T>G, NM_007332.2:c.1455T>G, XM_011517625.3:c.1455T>G, XM_011517625.2:c.1455T>G, XM_011517625.1:c.1455T>G, XM_011517624.3:c.1530T>G, XM_011517624.2:c.1530T>G, XM_011517624.1:c.1530T>G, NR_033652.1:n.4000A>C, NR_033651.1:n.3405A>C

Select item 148633372911.

rs1486333729 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:71963037 (GRCh38)
8:72875272 (GRCh37)
Canonical SPDI:: NC_000008.11:71963036:C:T
Gene:: MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.71963037C>T, NC_000008.10:g.72875272C>T, NR_033652.1:n.891C>T, NR_033651.1:n.422C>T

Select item 148599663712.

rs1485996637 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 8:72055418 (GRCh38)
8:72967653 (GRCh37)
Canonical SPDI:: NC_000008.11:72055417:CC:C
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.72055419del, NC_000008.10:g.72967654del, NG_033890.1:g.25167del, NR_033652.1:n.3909del, NR_033651.1:n.3314del

Select item 148571295913.

rs1485712959 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:72056231 (GRCh38)
8:72968466 (GRCh37)
Canonical SPDI:: NC_000008.11:72056230:T:C
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72056231T>C, NC_000008.10:g.72968466T>C, NG_033890.1:g.24354A>G, NR_033652.1:n.4721T>C, NR_033651.1:n.4126T>C

Select item 148455864014.

rs1484558640 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAGAGAAA>- [Show Flanks]
Chromosome:: 8:72053001 (GRCh38)
8:72965236 (GRCh37)
Canonical SPDI:: NC_000008.11:72052999:ATAGAGAAA:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000084/1 (ALFA)
-=0.000062/7 (GnomAD)
HGVS:: NC_000008.11:g.72053001_72053008del, NC_000008.10:g.72965236_72965243del, NG_033890.1:g.27578_27585del, NR_033652.1:n.1491_1498del, NR_033651.1:n.896_903del

Select item 148260134315.

rs1482601343 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:72053648 (GRCh38)
8:72965883 (GRCh37)
Canonical SPDI:: NC_000008.11:72053647:G:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.72053648G>A, NC_000008.10:g.72965883G>A, NG_033890.1:g.26937C>T, NR_033652.1:n.2138G>A, NR_033651.1:n.1543G>A

Select item 147975786116.

rs1479757861 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:72055176 (GRCh38)
8:72967411 (GRCh37)
Canonical SPDI:: NC_000008.11:72055175:G:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.72055176G>A, NC_000008.10:g.72967411G>A, NG_033890.1:g.25409C>T, NR_033652.1:n.3666G>A, NR_033651.1:n.3071G>A

Select item 147746314417.

rs1477463144 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 8:72054327 (GRCh38)
8:72966562 (GRCh37)
Canonical SPDI:: NC_000008.11:72054326:A:G,NC_000008.11:72054326:A:T
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000008.11:g.72054327A>G, NC_000008.11:g.72054327A>T, NC_000008.10:g.72966562A>G, NC_000008.10:g.72966562A>T, NG_033890.1:g.26258T>C, NG_033890.1:g.26258T>A, NR_033652.1:n.2817A>G, NR_033652.1:n.2817A>T, NR_033651.1:n.2222A>G, NR_033651.1:n.2222A>T

Select item 147716413118.

rs1477164131 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:72053199 (GRCh38)
8:72965434 (GRCh37)
Canonical SPDI:: NC_000008.11:72053198:G:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.72053199G>A, NC_000008.10:g.72965434G>A, NG_033890.1:g.27386C>T, NR_033652.1:n.1689G>A, NR_033651.1:n.1094G>A

Select item 147699572319.

rs1476995723 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:72054130 (GRCh38)
8:72966365 (GRCh37)
Canonical SPDI:: NC_000008.11:72054129:C:G
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.72054130C>G, NC_000008.10:g.72966365C>G, NG_033890.1:g.26455G>C, NR_033652.1:n.2620C>G, NR_033651.1:n.2025C>G

Select item 147613606920.

rs1476136069 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:72054605 (GRCh38)
8:72966840 (GRCh37)
Canonical SPDI:: NC_000008.11:72054604:C:A
Gene:: TRPA1 (Varview), MSC-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.72054605C>A, NC_000008.10:g.72966840C>A, NG_033890.1:g.25980G>T, NR_033652.1:n.3095C>A, NR_033651.1:n.2500C>A

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