SNP Links for Gene (Select 408) - SNP

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Select item 14915608121.

rs1491560812 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATATATA [Show Flanks]
Chromosome:: 11:75353800 (GRCh38)
11:75064845 (GRCh37)
Canonical SPDI:: NC_000011.10:75353800::A,NC_000011.10:75353800::ATA,NC_000011.10:75353800::ATATA,NC_000011.10:75353800::ATATATA,NC_000011.10:75353800::ATATATATA,NC_000011.10:75353800::ATATATATATA,NC_000011.10:75353800::ATATATATATATA,NC_000011.10:75353800::ATATATATATATATA,NC_000011.10:75353800::ATATATATATATATATATATA
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000011.10:g.75353800_75353801insA, NC_000011.10:g.75353800_75353801insATA, NC_000011.10:g.75353800_75353801insATATA, NC_000011.10:g.75353800_75353801insATATATA, NC_000011.10:g.75353800_75353801insATATATATA, NC_000011.10:g.75353800_75353801insATATATATATA, NC_000011.10:g.75353800_75353801insATATATATATATA, NC_000011.10:g.75353800_75353801insATATATATATATATA, NC_000011.10:g.75353800_75353801insATATATATATATATATATATA, NC_000011.9:g.75064844_75064845insA, NC_000011.9:g.75064844_75064845insATA, NC_000011.9:g.75064844_75064845insATATA, NC_000011.9:g.75064844_75064845insATATATA, NC_000011.9:g.75064844_75064845insATATATATA, NC_000011.9:g.75064844_75064845insATATATATATA, NC_000011.9:g.75064844_75064845insATATATATATATA, NC_000011.9:g.75064844_75064845insATATATATATATATA, NC_000011.9:g.75064844_75064845insATATATATATATATATATATA, NG_028118.1:g.3031_3032insT, NG_028118.1:g.3031_3032insTAT, NG_028118.1:g.3031_3032insTATAT, NG_028118.1:g.3031_3032insTATATAT, NG_028118.1:g.3031_3032insTATATATAT, NG_028118.1:g.3031_3032insTATATATATAT, NG_028118.1:g.3031_3032insTATATATATATAT, NG_028118.1:g.3031_3032insTATATATATATATAT, NG_028118.1:g.3031_3032insTATATATATATATATATATAT

Select item 14914448922.

rs1491444892 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->CAA
Chromosome:: no mapping
Canonical SPDI:

Select item 14913999243.

rs1491399924 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 11:75296186 (GRCh38)
11:75007231 (GRCh37)
Canonical SPDI:: NC_000011.10:75296186::G
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00097/26 (GnomAD)
HGVS:: NC_000011.10:g.75296186_75296187insG, NC_000011.9:g.75007230_75007231insG, NG_028118.1:g.60645_60646insC

Select item 14913363994.

rs1491336399 has merged into rs34831668 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:75297876 (GRCh38)
11:75008920 (GRCh37)
Canonical SPDI:: NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75297864:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000011.10:g.75297876_75297892del, NC_000011.10:g.75297878_75297892del, NC_000011.10:g.75297879_75297892del, NC_000011.10:g.75297880_75297892del, NC_000011.10:g.75297881_75297892del, NC_000011.10:g.75297882_75297892del, NC_000011.10:g.75297883_75297892del, NC_000011.10:g.75297884_75297892del, NC_000011.10:g.75297885_75297892del, NC_000011.10:g.75297886_75297892del, NC_000011.10:g.75297887_75297892del, NC_000011.10:g.75297888_75297892del, NC_000011.10:g.75297889_75297892del, NC_000011.10:g.75297890_75297892del, NC_000011.10:g.75297891_75297892del, NC_000011.10:g.75297892del, NC_000011.10:g.75297892dup, NC_000011.10:g.75297891_75297892dup, NC_000011.10:g.75297890_75297892dup, NC_000011.10:g.75297889_75297892dup, NC_000011.10:g.75297888_75297892dup, NC_000011.10:g.75297887_75297892dup, NC_000011.10:g.75297886_75297892dup, NC_000011.10:g.75297885_75297892dup, NC_000011.10:g.75297884_75297892dup, NC_000011.10:g.75297883_75297892dup, NC_000011.10:g.75297882_75297892dup, NC_000011.10:g.75297881_75297892dup, NC_000011.10:g.75297879_75297892dup, NC_000011.10:g.75297878_75297892dup, NC_000011.10:g.75297873_75297892dup, NC_000011.9:g.75008920_75008936del, NC_000011.9:g.75008922_75008936del, NC_000011.9:g.75008923_75008936del, NC_000011.9:g.75008924_75008936del, NC_000011.9:g.75008925_75008936del, NC_000011.9:g.75008926_75008936del, NC_000011.9:g.75008927_75008936del, NC_000011.9:g.75008928_75008936del, NC_000011.9:g.75008929_75008936del, NC_000011.9:g.75008930_75008936del, NC_000011.9:g.75008931_75008936del, NC_000011.9:g.75008932_75008936del, NC_000011.9:g.75008933_75008936del, NC_000011.9:g.75008934_75008936del, NC_000011.9:g.75008935_75008936del, NC_000011.9:g.75008936del, NC_000011.9:g.75008936dup, NC_000011.9:g.75008935_75008936dup, NC_000011.9:g.75008934_75008936dup, NC_000011.9:g.75008933_75008936dup, NC_000011.9:g.75008932_75008936dup, NC_000011.9:g.75008931_75008936dup, NC_000011.9:g.75008930_75008936dup, NC_000011.9:g.75008929_75008936dup, NC_000011.9:g.75008928_75008936dup, NC_000011.9:g.75008927_75008936dup, NC_000011.9:g.75008926_75008936dup, NC_000011.9:g.75008925_75008936dup, NC_000011.9:g.75008923_75008936dup, NC_000011.9:g.75008922_75008936dup, NC_000011.9:g.75008917_75008936dup, NG_028118.1:g.58951_58967del, NG_028118.1:g.58953_58967del, NG_028118.1:g.58954_58967del, NG_028118.1:g.58955_58967del, NG_028118.1:g.58956_58967del, NG_028118.1:g.58957_58967del, NG_028118.1:g.58958_58967del, NG_028118.1:g.58959_58967del, NG_028118.1:g.58960_58967del, NG_028118.1:g.58961_58967del, NG_028118.1:g.58962_58967del, NG_028118.1:g.58963_58967del, NG_028118.1:g.58964_58967del, NG_028118.1:g.58965_58967del, NG_028118.1:g.58966_58967del, NG_028118.1:g.58967del, NG_028118.1:g.58967dup, NG_028118.1:g.58966_58967dup, NG_028118.1:g.58965_58967dup, NG_028118.1:g.58964_58967dup, NG_028118.1:g.58963_58967dup, NG_028118.1:g.58962_58967dup, NG_028118.1:g.58961_58967dup, NG_028118.1:g.58960_58967dup, NG_028118.1:g.58959_58967dup, NG_028118.1:g.58958_58967dup, NG_028118.1:g.58957_58967dup, NG_028118.1:g.58956_58967dup, NG_028118.1:g.58954_58967dup, NG_028118.1:g.58953_58967dup, NG_028118.1:g.58948_58967dup

Select item 14913316525.

rs1491331652 has merged into rs1330209838 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:75353815 (GRCh38)
11:75064859 (GRCh37)
Canonical SPDI:: NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75353799:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75353815_75353822del, NC_000011.10:g.75353816_75353822del, NC_000011.10:g.75353817_75353822del, NC_000011.10:g.75353818_75353822del, NC_000011.10:g.75353819_75353822del, NC_000011.10:g.75353820_75353822del, NC_000011.10:g.75353821_75353822del, NC_000011.10:g.75353822del, NC_000011.10:g.75353822dup, NC_000011.10:g.75353821_75353822dup, NC_000011.10:g.75353820_75353822dup, NC_000011.10:g.75353818_75353822dup, NC_000011.10:g.75353817_75353822dup, NC_000011.9:g.75064859_75064866del, NC_000011.9:g.75064860_75064866del, NC_000011.9:g.75064861_75064866del, NC_000011.9:g.75064862_75064866del, NC_000011.9:g.75064863_75064866del, NC_000011.9:g.75064864_75064866del, NC_000011.9:g.75064865_75064866del, NC_000011.9:g.75064866del, NC_000011.9:g.75064866dup, NC_000011.9:g.75064865_75064866dup, NC_000011.9:g.75064864_75064866dup, NC_000011.9:g.75064862_75064866dup, NC_000011.9:g.75064861_75064866dup, NG_028118.1:g.3025_3032del, NG_028118.1:g.3026_3032del, NG_028118.1:g.3027_3032del, NG_028118.1:g.3028_3032del, NG_028118.1:g.3029_3032del, NG_028118.1:g.3030_3032del, NG_028118.1:g.3031_3032del, NG_028118.1:g.3032del, NG_028118.1:g.3032dup, NG_028118.1:g.3031_3032dup, NG_028118.1:g.3030_3032dup, NG_028118.1:g.3028_3032dup, NG_028118.1:g.3027_3032dup

Select item 14913057546.

rs1491305754 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:75295221 (GRCh38)
11:75006265 (GRCh37)
Canonical SPDI:: NC_000011.10:75295220:CA:
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01703/202 (ALFA)
-=0.00204/56 (TOMMO)
-=0.00332/123 (GnomAD)
HGVS:: NC_000011.10:g.75295221_75295222del, NC_000011.9:g.75006265_75006266del, NG_028118.1:g.61610_61611del

Select item 14912509777.

rs1491250977 has merged into rs11428462 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:75296195 (GRCh38)
11:75007239 (GRCh37)
Canonical SPDI:: NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75296185:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.000042/11 (TOPMED)
HGVS:: NC_000011.10:g.75296195_75296207del, NC_000011.10:g.75296196_75296207del, NC_000011.10:g.75296197_75296207del, NC_000011.10:g.75296198_75296207del, NC_000011.10:g.75296199_75296207del, NC_000011.10:g.75296200_75296207del, NC_000011.10:g.75296201_75296207del, NC_000011.10:g.75296202_75296207del, NC_000011.10:g.75296203_75296207del, NC_000011.10:g.75296204_75296207del, NC_000011.10:g.75296205_75296207del, NC_000011.10:g.75296206_75296207del, NC_000011.10:g.75296207del, NC_000011.10:g.75296207dup, NC_000011.10:g.75296206_75296207dup, NC_000011.10:g.75296205_75296207dup, NC_000011.10:g.75296204_75296207dup, NC_000011.10:g.75296203_75296207dup, NC_000011.10:g.75296202_75296207dup, NC_000011.10:g.75296201_75296207dup, NC_000011.10:g.75296189_75296207dup, NC_000011.10:g.75296187_75296207dup, NC_000011.9:g.75007239_75007251del, NC_000011.9:g.75007240_75007251del, NC_000011.9:g.75007241_75007251del, NC_000011.9:g.75007242_75007251del, NC_000011.9:g.75007243_75007251del, NC_000011.9:g.75007244_75007251del, NC_000011.9:g.75007245_75007251del, NC_000011.9:g.75007246_75007251del, NC_000011.9:g.75007247_75007251del, NC_000011.9:g.75007248_75007251del, NC_000011.9:g.75007249_75007251del, NC_000011.9:g.75007250_75007251del, NC_000011.9:g.75007251del, NC_000011.9:g.75007251dup, NC_000011.9:g.75007250_75007251dup, NC_000011.9:g.75007249_75007251dup, NC_000011.9:g.75007248_75007251dup, NC_000011.9:g.75007247_75007251dup, NC_000011.9:g.75007246_75007251dup, NC_000011.9:g.75007245_75007251dup, NC_000011.9:g.75007233_75007251dup, NC_000011.9:g.75007231_75007251dup, NG_028118.1:g.60634_60646del, NG_028118.1:g.60635_60646del, NG_028118.1:g.60636_60646del, NG_028118.1:g.60637_60646del, NG_028118.1:g.60638_60646del, NG_028118.1:g.60639_60646del, NG_028118.1:g.60640_60646del, NG_028118.1:g.60641_60646del, NG_028118.1:g.60642_60646del, NG_028118.1:g.60643_60646del, NG_028118.1:g.60644_60646del, NG_028118.1:g.60645_60646del, NG_028118.1:g.60646del, NG_028118.1:g.60646dup, NG_028118.1:g.60645_60646dup, NG_028118.1:g.60644_60646dup, NG_028118.1:g.60643_60646dup, NG_028118.1:g.60642_60646dup, NG_028118.1:g.60641_60646dup, NG_028118.1:g.60640_60646dup, NG_028118.1:g.60628_60646dup, NG_028118.1:g.60626_60646dup

Select item 14911866198.

rs1491186619 has merged into rs35323331 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:75305025 (GRCh38)
11:75016069 (GRCh37)
Canonical SPDI:: NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:75305018:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
HGVS:: NC_000011.10:g.75305025_75305040del, NC_000011.10:g.75305028_75305040del, NC_000011.10:g.75305029_75305040del, NC_000011.10:g.75305030_75305040del, NC_000011.10:g.75305031_75305040del, NC_000011.10:g.75305032_75305040del, NC_000011.10:g.75305033_75305040del, NC_000011.10:g.75305034_75305040del, NC_000011.10:g.75305035_75305040del, NC_000011.10:g.75305036_75305040del, NC_000011.10:g.75305037_75305040del, NC_000011.10:g.75305038_75305040del, NC_000011.10:g.75305039_75305040del, NC_000011.10:g.75305040del, NC_000011.10:g.75305040dup, NC_000011.10:g.75305039_75305040dup, NC_000011.10:g.75305019_75305040T[24]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.75305019_75305040T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.10:g.75305038_75305040dup, NC_000011.10:g.75305036_75305040dup, NC_000011.10:g.75305035_75305040dup, NC_000011.10:g.75305034_75305040dup, NC_000011.10:g.75305032_75305040dup, NC_000011.10:g.75305031_75305040dup, NC_000011.10:g.75305030_75305040dup, NC_000011.10:g.75305029_75305040dup, NC_000011.10:g.75305028_75305040dup, NC_000011.10:g.75305027_75305040dup, NC_000011.10:g.75305026_75305040dup, NC_000011.10:g.75305025_75305040dup, NC_000011.10:g.75305024_75305040dup, NC_000011.10:g.75305023_75305040dup, NC_000011.10:g.75305022_75305040dup, NC_000011.10:g.75305021_75305040dup, NC_000011.10:g.75305020_75305040dup, NC_000011.10:g.75305019_75305040dup, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.10:g.75305040_75305041insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016069_75016084del, NC_000011.9:g.75016072_75016084del, NC_000011.9:g.75016073_75016084del, NC_000011.9:g.75016074_75016084del, NC_000011.9:g.75016075_75016084del, NC_000011.9:g.75016076_75016084del, NC_000011.9:g.75016077_75016084del, NC_000011.9:g.75016078_75016084del, NC_000011.9:g.75016079_75016084del, NC_000011.9:g.75016080_75016084del, NC_000011.9:g.75016081_75016084del, NC_000011.9:g.75016082_75016084del, NC_000011.9:g.75016083_75016084del, NC_000011.9:g.75016084del, NC_000011.9:g.75016084dup, NC_000011.9:g.75016083_75016084dup, NC_000011.9:g.75016063_75016084T[24]ATTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.75016063_75016084T[24]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000011.9:g.75016082_75016084dup, NC_000011.9:g.75016080_75016084dup, NC_000011.9:g.75016079_75016084dup, NC_000011.9:g.75016078_75016084dup, NC_000011.9:g.75016076_75016084dup, NC_000011.9:g.75016075_75016084dup, NC_000011.9:g.75016074_75016084dup, NC_000011.9:g.75016073_75016084dup, NC_000011.9:g.75016072_75016084dup, NC_000011.9:g.75016071_75016084dup, NC_000011.9:g.75016070_75016084dup, NC_000011.9:g.75016069_75016084dup, NC_000011.9:g.75016068_75016084dup, NC_000011.9:g.75016067_75016084dup, NC_000011.9:g.75016066_75016084dup, NC_000011.9:g.75016065_75016084dup, NC_000011.9:g.75016064_75016084dup, NC_000011.9:g.75016063_75016084dup, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000011.9:g.75016084_75016085insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_028118.1:g.51798_51813del, NG_028118.1:g.51801_51813del, NG_028118.1:g.51802_51813del, NG_028118.1:g.51803_51813del, NG_028118.1:g.51804_51813del, NG_028118.1:g.51805_51813del, NG_028118.1:g.51806_51813del, NG_028118.1:g.51807_51813del, NG_028118.1:g.51808_51813del, NG_028118.1:g.51809_51813del, NG_028118.1:g.51810_51813del, NG_028118.1:g.51811_51813del, NG_028118.1:g.51812_51813del, NG_028118.1:g.51813del, NG_028118.1:g.51813dup, NG_028118.1:g.51812_51813dup, NG_028118.1:g.51792_51813A[23]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_028118.1:g.51792_51813A[26]TAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_028118.1:g.51811_51813dup, NG_028118.1:g.51809_51813dup, NG_028118.1:g.51808_51813dup, NG_028118.1:g.51807_51813dup, NG_028118.1:g.51805_51813dup, NG_028118.1:g.51804_51813dup, NG_028118.1:g.51803_51813dup, NG_028118.1:g.51802_51813dup, NG_028118.1:g.51801_51813dup, NG_028118.1:g.51800_51813dup, NG_028118.1:g.51799_51813dup, NG_028118.1:g.51798_51813dup, NG_028118.1:g.51797_51813dup, NG_028118.1:g.51796_51813dup, NG_028118.1:g.51795_51813dup, NG_028118.1:g.51794_51813dup, NG_028118.1:g.51793_51813dup, NG_028118.1:g.51792_51813dup, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028118.1:g.51813_51814insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14910891849.

rs1491089184 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 11:75288618 (GRCh38)
11:74999663 (GRCh37)
Canonical SPDI:: NC_000011.10:75288618:T:TCT
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCT=0./0 (ALFA)
TC=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75288619_75288620insCT, NC_000011.9:g.74999663_74999664insCT, NG_028118.1:g.68213_68214insGA

Select item 149107187710.

rs1491071877 has merged into rs34666904 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:75295233 (GRCh38)
11:75006277 (GRCh37)
Canonical SPDI:: NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:75295221:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75295233_75295246del, NC_000011.10:g.75295234_75295246del, NC_000011.10:g.75295235_75295246del, NC_000011.10:g.75295237_75295246del, NC_000011.10:g.75295238_75295246del, NC_000011.10:g.75295239_75295246del, NC_000011.10:g.75295240_75295246del, NC_000011.10:g.75295242_75295246del, NC_000011.10:g.75295243_75295246del, NC_000011.10:g.75295244_75295246del, NC_000011.10:g.75295245_75295246del, NC_000011.10:g.75295246del, NC_000011.10:g.75295246dup, NC_000011.10:g.75295245_75295246dup, NC_000011.10:g.75295244_75295246dup, NC_000011.10:g.75295243_75295246dup, NC_000011.10:g.75295242_75295246dup, NC_000011.10:g.75295241_75295246dup, NC_000011.10:g.75295240_75295246dup, NC_000011.9:g.75006277_75006290del, NC_000011.9:g.75006278_75006290del, NC_000011.9:g.75006279_75006290del, NC_000011.9:g.75006281_75006290del, NC_000011.9:g.75006282_75006290del, NC_000011.9:g.75006283_75006290del, NC_000011.9:g.75006284_75006290del, NC_000011.9:g.75006286_75006290del, NC_000011.9:g.75006287_75006290del, NC_000011.9:g.75006288_75006290del, NC_000011.9:g.75006289_75006290del, NC_000011.9:g.75006290del, NC_000011.9:g.75006290dup, NC_000011.9:g.75006289_75006290dup, NC_000011.9:g.75006288_75006290dup, NC_000011.9:g.75006287_75006290dup, NC_000011.9:g.75006286_75006290dup, NC_000011.9:g.75006285_75006290dup, NC_000011.9:g.75006284_75006290dup, NG_028118.1:g.61597_61610del, NG_028118.1:g.61598_61610del, NG_028118.1:g.61599_61610del, NG_028118.1:g.61601_61610del, NG_028118.1:g.61602_61610del, NG_028118.1:g.61603_61610del, NG_028118.1:g.61604_61610del, NG_028118.1:g.61606_61610del, NG_028118.1:g.61607_61610del, NG_028118.1:g.61608_61610del, NG_028118.1:g.61609_61610del, NG_028118.1:g.61610del, NG_028118.1:g.61610dup, NG_028118.1:g.61609_61610dup, NG_028118.1:g.61608_61610dup, NG_028118.1:g.61607_61610dup, NG_028118.1:g.61606_61610dup, NG_028118.1:g.61605_61610dup, NG_028118.1:g.61604_61610dup

Select item 149102340311.

rs1491023403 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 11:75295245 (GRCh38)
11:75006290 (GRCh37)
Canonical SPDI:: NC_000011.10:75295245::C
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000033/4 (GnomAD)
C=0.001494/25 (TOMMO)
HGVS:: NC_000011.10:g.75295245_75295246insC, NC_000011.9:g.75006289_75006290insC, NG_028118.1:g.61586_61587insG

Select item 149097872312.

rs1490978723 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:75344759 (GRCh38)
11:75055803 (GRCh37)
Canonical SPDI:: NC_000011.10:75344758:C:A
Gene:: ARRB1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.75344759C>A, NC_000011.9:g.75055803C>A, NG_028118.1:g.12073G>T

Select item 149094554213.

rs1490945542 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75290645 (GRCh38)
11:75001689 (GRCh37)
Canonical SPDI:: NC_000011.10:75290644:T:C
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75290645T>C, NC_000011.9:g.75001689T>C, NG_028118.1:g.66187A>G

Select item 149094193514.

rs1490941935 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 11:75261359 (GRCh38)
11:74972404 (GRCh37)
Canonical SPDI:: NC_000011.10:75261359:TTT:TTTT
Gene:: ARRB1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.75261362dup, NC_000011.9:g.74972406dup, NG_028118.1:g.95472dup, NM_004041.5:c.*4803dup, NM_004041.4:c.*4803dup, NM_020251.4:c.*4803dup, NM_020251.3:c.*4803dup, XM_017017752.3:c.*4803dup, XM_017017752.2:c.*4803dup, XM_017017752.1:c.*4803dup, XM_017017754.3:c.*4803dup, XM_017017754.2:c.*4803dup, XM_017017754.1:c.*4803dup, XM_011545034.2:c.*4803dup, XM_011545035.2:c.*4803dup, XM_017017753.1:c.*4803dup, XM_017017750.1:c.*4803dup, XM_017017751.1:c.*4803dup

Select item 149092334315.

rs1490923343 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75275775 (GRCh38)
11:74986819 (GRCh37)
Canonical SPDI:: NC_000011.10:75275774:C:T
Gene:: ARRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75275775C>T, NC_000011.9:g.74986819C>T, NG_028118.1:g.81057G>A

Select item 149090776116.

rs1490907761 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:75345734 (GRCh38)
11:75056778 (GRCh37)
Canonical SPDI:: NC_000011.10:75345733:C:A,NC_000011.10:75345733:C:T
Gene:: ARRB1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.75345734C>A, NC_000011.10:g.75345734C>T, NC_000011.9:g.75056778C>A, NC_000011.9:g.75056778C>T, NG_028118.1:g.11098G>T, NG_028118.1:g.11098G>A

Select item 149083588417.

rs1490835884 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75353490 (GRCh38)
11:75064534 (GRCh37)
Canonical SPDI:: NC_000011.10:75353489:C:T
Gene:: ARRB1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75353490C>T, NC_000011.9:g.75064534C>T, NG_028118.1:g.3342G>A

Select item 149080574418.

rs1490805744 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:75314819 (GRCh38)
11:75025863 (GRCh37)
Canonical SPDI:: NC_000011.10:75314818:C:G,NC_000011.10:75314818:C:T
Gene:: ARRB1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000021/3 (GnomAD)
G=0.001667/1 (NorthernSweden)
HGVS:: NC_000011.10:g.75314819C>G, NC_000011.10:g.75314819C>T, NC_000011.9:g.75025863C>G, NC_000011.9:g.75025863C>T, NG_028118.1:g.42013G>C, NG_028118.1:g.42013G>A

Select item 149079459319.

rs1490794593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75313449 (GRCh38)
11:75024493 (GRCh37)
Canonical SPDI:: NC_000011.10:75313448:G:A
Gene:: ARRB1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.75313449G>A, NC_000011.9:g.75024493G>A, NG_028118.1:g.43383C>T

Select item 149072212520.

rs1490722125 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:75260519 (GRCh38)
11:74971563 (GRCh37)
Canonical SPDI:: NC_000011.10:75260518:C:A
Gene:: ARRB1 (Varview)
Functional Consequence:: 3_prime_UTR_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_000011.10:g.75260519C>A, NC_000011.9:g.74971563C>A, NG_028118.1:g.96313G>T, NM_004041.5:c.*5644G>T, NM_004041.4:c.*5644G>T, NM_020251.4:c.*5644G>T, NM_020251.3:c.*5644G>T, XM_017017752.3:c.*5644G>T, XM_017017752.2:c.*5644G>T, XM_017017752.1:c.*5644G>T, XM_017017754.3:c.*5644G>T, XM_017017754.2:c.*5644G>T, XM_017017754.1:c.*5644G>T, XM_011545034.2:c.*5644G>T, XM_011545035.2:c.*5644G>T, XM_017017753.1:c.*5644G>T, XM_017017750.1:c.*5644G>T, XM_017017751.1:c.*5644G>T

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