SNP Links for Gene (Select 55717) - SNP

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Select item 14914059471.

rs1491405947 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:120858133 (GRCh38)
10:122617645 (GRCh37)
Canonical SPDI:: NC_000010.11:120858132:AT:
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.120858133_120858134del, NC_000010.10:g.122617645_122617646del, NG_023290.1:g.11959_11960del

Select item 14913277712.

rs1491327771 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTT [Show Flanks]
Chromosome:: 10:120874177 (GRCh38)
10:122633690 (GRCh37)
Canonical SPDI:: NC_000010.11:120874177:TT:TTGTT
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTGTT=0./0 (ALFA)
TTG=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.120874179_120874180insGTT, NC_000010.10:g.122633691_122633692insGTT, NG_023290.1:g.28005_28006insGTT

Select item 14913031343.

rs1491303134 has merged into rs35675368 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:120869118 (GRCh38)
10:122628630 (GRCh37)
Canonical SPDI:: NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.120869118_120869128del, NC_000010.11:g.120869119_120869128del, NC_000010.11:g.120869124_120869128del, NC_000010.11:g.120869126_120869128del, NC_000010.11:g.120869127_120869128del, NC_000010.11:g.120869128del, NC_000010.11:g.120869128dup, NC_000010.11:g.120869127_120869128dup, NC_000010.11:g.120869126_120869128dup, NC_000010.11:g.120869125_120869128dup, NC_000010.11:g.120869124_120869128dup, NC_000010.11:g.120869123_120869128dup, NC_000010.11:g.120869122_120869128dup, NC_000010.11:g.120869121_120869128dup, NC_000010.11:g.120869128_120869129insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628630_122628640del, NC_000010.10:g.122628631_122628640del, NC_000010.10:g.122628636_122628640del, NC_000010.10:g.122628638_122628640del, NC_000010.10:g.122628639_122628640del, NC_000010.10:g.122628640del, NC_000010.10:g.122628640dup, NC_000010.10:g.122628639_122628640dup, NC_000010.10:g.122628638_122628640dup, NC_000010.10:g.122628637_122628640dup, NC_000010.10:g.122628636_122628640dup, NC_000010.10:g.122628635_122628640dup, NC_000010.10:g.122628634_122628640dup, NC_000010.10:g.122628633_122628640dup, NC_000010.10:g.122628640_122628641insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22944_22954del, NG_023290.1:g.22945_22954del, NG_023290.1:g.22950_22954del, NG_023290.1:g.22952_22954del, NG_023290.1:g.22953_22954del, NG_023290.1:g.22954del, NG_023290.1:g.22954dup, NG_023290.1:g.22953_22954dup, NG_023290.1:g.22952_22954dup, NG_023290.1:g.22951_22954dup, NG_023290.1:g.22950_22954dup, NG_023290.1:g.22949_22954dup, NG_023290.1:g.22948_22954dup, NG_023290.1:g.22947_22954dup, NG_023290.1:g.22954_22955insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14912979574.

rs1491297957 has merged into rs34379642 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT [Show Flanks]
Chromosome:: 10:120858144 (GRCh38)
10:122617656 (GRCh37)
Canonical SPDI:: NC_000010.11:120858133:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:120858133:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:120858133:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:120858133:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:120858133:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.3531/1361 (ALSPAC)
-=0.4753/1682 (1000Genomes)
HGVS:: NC_000010.11:g.120858144_120858146del, NC_000010.11:g.120858145_120858146del, NC_000010.11:g.120858146del, NC_000010.11:g.120858146dup, NC_000010.11:g.120858145_120858146dup, NC_000010.10:g.122617656_122617658del, NC_000010.10:g.122617657_122617658del, NC_000010.10:g.122617658del, NC_000010.10:g.122617658dup, NC_000010.10:g.122617657_122617658dup, NG_023290.1:g.11970_11972del, NG_023290.1:g.11971_11972del, NG_023290.1:g.11972del, NG_023290.1:g.11972dup, NG_023290.1:g.11971_11972dup

Select item 14911371835.

rs1491137183 has merged into rs35675368 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:120869118 (GRCh38)
10:122628630 (GRCh37)
Canonical SPDI:: NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869106:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.120869118_120869128del, NC_000010.11:g.120869119_120869128del, NC_000010.11:g.120869124_120869128del, NC_000010.11:g.120869126_120869128del, NC_000010.11:g.120869127_120869128del, NC_000010.11:g.120869128del, NC_000010.11:g.120869128dup, NC_000010.11:g.120869127_120869128dup, NC_000010.11:g.120869126_120869128dup, NC_000010.11:g.120869125_120869128dup, NC_000010.11:g.120869124_120869128dup, NC_000010.11:g.120869123_120869128dup, NC_000010.11:g.120869122_120869128dup, NC_000010.11:g.120869121_120869128dup, NC_000010.11:g.120869128_120869129insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628630_122628640del, NC_000010.10:g.122628631_122628640del, NC_000010.10:g.122628636_122628640del, NC_000010.10:g.122628638_122628640del, NC_000010.10:g.122628639_122628640del, NC_000010.10:g.122628640del, NC_000010.10:g.122628640dup, NC_000010.10:g.122628639_122628640dup, NC_000010.10:g.122628638_122628640dup, NC_000010.10:g.122628637_122628640dup, NC_000010.10:g.122628636_122628640dup, NC_000010.10:g.122628635_122628640dup, NC_000010.10:g.122628634_122628640dup, NC_000010.10:g.122628633_122628640dup, NC_000010.10:g.122628640_122628641insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22944_22954del, NG_023290.1:g.22945_22954del, NG_023290.1:g.22950_22954del, NG_023290.1:g.22952_22954del, NG_023290.1:g.22953_22954del, NG_023290.1:g.22954del, NG_023290.1:g.22954dup, NG_023290.1:g.22953_22954dup, NG_023290.1:g.22952_22954dup, NG_023290.1:g.22951_22954dup, NG_023290.1:g.22950_22954dup, NG_023290.1:g.22949_22954dup, NG_023290.1:g.22948_22954dup, NG_023290.1:g.22947_22954dup, NG_023290.1:g.22954_22955insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14910375866.

rs1491037586 has merged into rs71019798 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,A,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:120856587 (GRCh38)
10:122616099 (GRCh37)
Canonical SPDI:: NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:120856575:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.120856587_120856596del, NC_000010.11:g.120856588_120856596del, NC_000010.11:g.120856590_120856596del, NC_000010.11:g.120856592_120856596del, NC_000010.11:g.120856593_120856596del, NC_000010.11:g.120856594_120856596del, NC_000010.11:g.120856595_120856596del, NC_000010.11:g.120856596del, NC_000010.11:g.120856596dup, NC_000010.11:g.120856595_120856596dup, NC_000010.11:g.120856594_120856596dup, NC_000010.11:g.120856593_120856596dup, NC_000010.11:g.120856592_120856596dup, NC_000010.11:g.120856590_120856596dup, NC_000010.11:g.120856576_120856596A[23]CAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000010.10:g.122616099_122616108del, NC_000010.10:g.122616100_122616108del, NC_000010.10:g.122616102_122616108del, NC_000010.10:g.122616104_122616108del, NC_000010.10:g.122616105_122616108del, NC_000010.10:g.122616106_122616108del, NC_000010.10:g.122616107_122616108del, NC_000010.10:g.122616108del, NC_000010.10:g.122616108dup, NC_000010.10:g.122616107_122616108dup, NC_000010.10:g.122616106_122616108dup, NC_000010.10:g.122616105_122616108dup, NC_000010.10:g.122616104_122616108dup, NC_000010.10:g.122616102_122616108dup, NC_000010.10:g.122616088_122616108A[23]CAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_023290.1:g.10413_10422del, NG_023290.1:g.10414_10422del, NG_023290.1:g.10416_10422del, NG_023290.1:g.10418_10422del, NG_023290.1:g.10419_10422del, NG_023290.1:g.10420_10422del, NG_023290.1:g.10421_10422del, NG_023290.1:g.10422del, NG_023290.1:g.10422dup, NG_023290.1:g.10421_10422dup, NG_023290.1:g.10420_10422dup, NG_023290.1:g.10419_10422dup, NG_023290.1:g.10418_10422dup, NG_023290.1:g.10416_10422dup, NG_023290.1:g.10402_10422A[23]CAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 14910356227.

rs1491035622 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:120869105 (GRCh38)
10:122628618 (GRCh37)
Canonical SPDI:: NC_000010.11:120869105::T,NC_000010.11:120869105::TT,NC_000010.11:120869105::TTT,NC_000010.11:120869105::TTTT,NC_000010.11:120869105::TTTTT,NC_000010.11:120869105::TTTTTT,NC_000010.11:120869105::TTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:120869105::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
HGVS:: NC_000010.11:g.120869105_120869106insT, NC_000010.11:g.120869105_120869106insTT, NC_000010.11:g.120869105_120869106insTTT, NC_000010.11:g.120869105_120869106insTTTT, NC_000010.11:g.120869105_120869106insTTTTT, NC_000010.11:g.120869105_120869106insTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.120869105_120869106insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insT, NC_000010.10:g.122628617_122628618insTT, NC_000010.10:g.122628617_122628618insTTT, NC_000010.10:g.122628617_122628618insTTTT, NC_000010.10:g.122628617_122628618insTTTTT, NC_000010.10:g.122628617_122628618insTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.122628617_122628618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insT, NG_023290.1:g.22931_22932insTT, NG_023290.1:g.22931_22932insTTT, NG_023290.1:g.22931_22932insTTTT, NG_023290.1:g.22931_22932insTTTTT, NG_023290.1:g.22931_22932insTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_023290.1:g.22931_22932insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14910005678.

rs1491000567 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:120865829 (GRCh38)
10:122625341 (GRCh37)
Canonical SPDI:: NC_000010.11:120865828:A:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.120865829A>G, NC_000010.10:g.122625341A>G, NG_023290.1:g.19655A>G

Select item 14909646609.

rs1490964660 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:120868732 (GRCh38)
10:122628244 (GRCh37)
Canonical SPDI:: NC_000010.11:120868731:C:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.120868732C>G, NC_000010.10:g.122628244C>G, NG_023290.1:g.22558C>G

Select item 149089044210.

rs1490890442 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:120870489 (GRCh38)
10:122630001 (GRCh37)
Canonical SPDI:: NC_000010.11:120870488:T:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000036/5 (GnomAD)
G=0.000049/13 (TOPMED)
HGVS:: NC_000010.11:g.120870489T>G, NC_000010.10:g.122630001T>G, NG_023290.1:g.24315T>G

Select item 149082365111.

rs1490823651 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:120863253 (GRCh38)
10:122622765 (GRCh37)
Canonical SPDI:: NC_000010.11:120863252:A:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.120863253A>G, NC_000010.10:g.122622765A>G, NG_023290.1:g.17079A>G

Select item 149080107912.

rs1490801079 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:120877463 (GRCh38)
10:122636975 (GRCh37)
Canonical SPDI:: NC_000010.11:120877462:A:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.120877463A>G, NC_000010.10:g.122636975A>G, NG_023290.1:g.31289A>G

Select item 149079392313.

rs1490793923 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:120906667 (GRCh38)
10:122666179 (GRCh37)
Canonical SPDI:: NC_000010.11:120906666:T:C
Gene:: WDR11 (Varview), LOC105378519 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
HGVS:: NC_000010.11:g.120906667T>C, NC_000010.10:g.122666179T>C, NG_023290.1:g.60493T>C

Select item 149076820914.

rs1490768209 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:120862091 (GRCh38)
10:122621603 (GRCh37)
Canonical SPDI:: NC_000010.11:120862090:A:C
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.120862091A>C, NC_000010.10:g.122621603A>C, NG_023290.1:g.15917A>C

Select item 149075015115.

rs1490750151 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:120878658 (GRCh38)
10:122638170 (GRCh37)
Canonical SPDI:: NC_000010.11:120878657:A:G
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.120878658A>G, NC_000010.10:g.122638170A>G, NG_023290.1:g.32484A>G

Select item 149073805416.

rs1490738054 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:120894564 (GRCh38)
10:122654076 (GRCh37)
Canonical SPDI:: NC_000010.11:120894563:T:C
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
C=0.000248/4 (TOMMO)
HGVS:: NC_000010.11:g.120894564T>C, NC_000010.10:g.122654076T>C, NG_023290.1:g.48390T>C

Select item 149061587717.

rs1490615877 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:120865684 (GRCh38)
10:122625196 (GRCh37)
Canonical SPDI:: NC_000010.11:120865683:A:G
Gene:: WDR11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.120865684A>G, NC_000010.10:g.122625196A>G, NG_023290.1:g.19510A>G, NM_018117.12:c.934A>G, NM_018117.11:c.934A>G, XR_428707.4:n.993A>G, XR_428707.3:n.1015A>G, XR_428707.2:n.1071A>G, XR_428707.1:n.1071A>G, XM_005269963.3:c.157A>G, XM_005269963.2:c.157A>G, XM_005269963.1:c.157A>G, XM_047425459.1:c.157A>G, XM_047425458.1:c.157A>G, XR_007061973.1:n.993A>G, NP_060587.8:p.Ile312Val, XP_005270020.1:p.Ile53Val, XP_047281415.1:p.Ile53Val, XP_047281414.1:p.Ile53Val

Select item 149059071918.

rs1490590719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:120905553 (GRCh38)
10:122665065 (GRCh37)
Canonical SPDI:: NC_000010.11:120905552:C:G,NC_000010.11:120905552:C:T
Gene:: WDR11 (Varview), LOC105378519 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.120905553C>G, NC_000010.11:g.120905553C>T, NC_000010.10:g.122665065C>G, NC_000010.10:g.122665065C>T, NG_023290.1:g.59379C>G, NG_023290.1:g.59379C>T

Select item 149058752019.

rs1490587520 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:120879171 (GRCh38)
10:122638683 (GRCh37)
Canonical SPDI:: NC_000010.11:120879170:T:C
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.120879171T>C, NC_000010.10:g.122638683T>C, NG_023290.1:g.32997T>C

Select item 149054762220.

rs1490547622 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:120864947 (GRCh38)
10:122624459 (GRCh37)
Canonical SPDI:: NC_000010.11:120864946:T:C
Gene:: WDR11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.120864947T>C, NC_000010.10:g.122624459T>C, NG_023290.1:g.18773T>C

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