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Select item 14915742461.

rs1491574246 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CACACA,CACACACACACA [Show Flanks]
Chromosome:: 13:26268254 (GRCh38)
13:26842392 (GRCh37)
Canonical SPDI:: NC_000013.11:26268254:CA:CACACACA,NC_000013.11:26268254:CA:CACACACACACACA
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000013.11:g.26268255CA[4], NC_000013.11:g.26268255CA[7], NC_000013.10:g.26842392CA[4], NC_000013.10:g.26842392CA[7]

Select item 14915379782.

rs1491537978 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:26279989 (GRCh38)
13:26854126 (GRCh37)
Canonical SPDI:: NC_000013.11:26279987:TAT:T
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000169/2 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.26279989_26279990del, NC_000013.10:g.26854126_26854127del

Select item 14914446043.

rs1491444604 has merged into rs59801630 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 13:26284953 (GRCh38)
13:26859090 (GRCh37)
Canonical SPDI:: NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:26284942:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
Gene:: CDK8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
A=0.0453/168 (TWINSUK)
A=0.0454/175 (ALSPAC)
HGVS:: NC_000013.11:g.26284953_26284956del, NC_000013.11:g.26284954_26284956del, NC_000013.11:g.26284955_26284956del, NC_000013.11:g.26284956del, NC_000013.11:g.26284956dup, NC_000013.11:g.26284955_26284956dup, NC_000013.11:g.26284954_26284956dup, NC_000013.11:g.26284953_26284956dup, NC_000013.10:g.26859090_26859093del, NC_000013.10:g.26859091_26859093del, NC_000013.10:g.26859092_26859093del, NC_000013.10:g.26859093del, NC_000013.10:g.26859093dup, NC_000013.10:g.26859092_26859093dup, NC_000013.10:g.26859091_26859093dup, NC_000013.10:g.26859090_26859093dup

Select item 14914114714.

rs1491411471 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 13:26329482 (GRCh38)
13:26903620 (GRCh37)
Canonical SPDI:: NC_000013.11:26329482:G:GG
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000013.11:g.26329483dup, NC_000013.10:g.26903620dup

Select item 14913957945.

rs1491395794 has merged into rs36116401 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:26369715 (GRCh38)
13:26943852 (GRCh37)
Canonical SPDI:: NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000013.11:26369709:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CDK8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
HGVS:: NC_000013.11:g.26369715_26369729del, NC_000013.11:g.26369718_26369729del, NC_000013.11:g.26369719_26369729del, NC_000013.11:g.26369720_26369729del, NC_000013.11:g.26369721_26369729del, NC_000013.11:g.26369722_26369729del, NC_000013.11:g.26369723_26369729del, NC_000013.11:g.26369724_26369729del, NC_000013.11:g.26369725_26369729del, NC_000013.11:g.26369726_26369729del, NC_000013.11:g.26369727_26369729del, NC_000013.11:g.26369728_26369729del, NC_000013.11:g.26369729del, NC_000013.11:g.26369729dup, NC_000013.11:g.26369728_26369729dup, NC_000013.11:g.26369727_26369729dup, NC_000013.11:g.26369726_26369729dup, NC_000013.11:g.26369725_26369729dup, NC_000013.11:g.26369724_26369729dup, NC_000013.11:g.26369723_26369729dup, NC_000013.11:g.26369722_26369729dup, NC_000013.11:g.26369721_26369729dup, NC_000013.11:g.26369720_26369729dup, NC_000013.11:g.26369719_26369729dup, NC_000013.11:g.26369718_26369729dup, NC_000013.11:g.26369717_26369729dup, NC_000013.11:g.26369716_26369729dup, NC_000013.11:g.26369715_26369729dup, NC_000013.11:g.26369714_26369729dup, NC_000013.11:g.26369713_26369729dup, NC_000013.11:g.26369712_26369729dup, NC_000013.10:g.26943852_26943866del, NC_000013.10:g.26943855_26943866del, NC_000013.10:g.26943856_26943866del, NC_000013.10:g.26943857_26943866del, NC_000013.10:g.26943858_26943866del, NC_000013.10:g.26943859_26943866del, NC_000013.10:g.26943860_26943866del, NC_000013.10:g.26943861_26943866del, NC_000013.10:g.26943862_26943866del, NC_000013.10:g.26943863_26943866del, NC_000013.10:g.26943864_26943866del, NC_000013.10:g.26943865_26943866del, NC_000013.10:g.26943866del, NC_000013.10:g.26943866dup, NC_000013.10:g.26943865_26943866dup, NC_000013.10:g.26943864_26943866dup, NC_000013.10:g.26943863_26943866dup, NC_000013.10:g.26943862_26943866dup, NC_000013.10:g.26943861_26943866dup, NC_000013.10:g.26943860_26943866dup, NC_000013.10:g.26943859_26943866dup, NC_000013.10:g.26943858_26943866dup, NC_000013.10:g.26943857_26943866dup, NC_000013.10:g.26943856_26943866dup, NC_000013.10:g.26943855_26943866dup, NC_000013.10:g.26943854_26943866dup, NC_000013.10:g.26943853_26943866dup, NC_000013.10:g.26943852_26943866dup, NC_000013.10:g.26943851_26943866dup, NC_000013.10:g.26943850_26943866dup, NC_000013.10:g.26943849_26943866dup

Select item 14913718026.

rs1491371802 has merged into rs71080250 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTTTTTTT [Show Flanks]
Chromosome:: 13:26309154 (GRCh38)
13:26883291 (GRCh37)
Canonical SPDI:: NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000013.11:26309141:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CDK8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0.0131/59 (ALFA)
T=0.0116/43 (TWINSUK)
T=0.0125/48 (ALSPAC)
T=0.0935/468 (1000Genomes)
HGVS:: NC_000013.11:g.26309154_26309157del, NC_000013.11:g.26309155_26309157del, NC_000013.11:g.26309156_26309157del, NC_000013.11:g.26309157del, NC_000013.11:g.26309157dup, NC_000013.11:g.26309156_26309157dup, NC_000013.11:g.26309150_26309157dup, NC_000013.10:g.26883291_26883294del, NC_000013.10:g.26883292_26883294del, NC_000013.10:g.26883293_26883294del, NC_000013.10:g.26883294del, NC_000013.10:g.26883294dup, NC_000013.10:g.26883293_26883294dup, NC_000013.10:g.26883287_26883294dup

Select item 14913671027.

rs1491367102 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 13:26335919 (GRCh38)
13:26910056 (GRCh37)
Canonical SPDI:: NC_000013.11:26335918:TT:
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00003/2 (GnomAD)
HGVS:: NC_000013.11:g.26335919_26335920del, NC_000013.10:g.26910056_26910057del

Select item 14913205098.

rs1491320509 has merged into rs67551273 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:26252136 (GRCh38)
13:26826273 (GRCh37)
Canonical SPDI:: NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26252125:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: CDK8 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.26252136_26252147del, NC_000013.11:g.26252138_26252147del, NC_000013.11:g.26252139_26252147del, NC_000013.11:g.26252141_26252147del, NC_000013.11:g.26252142_26252147del, NC_000013.11:g.26252143_26252147del, NC_000013.11:g.26252144_26252147del, NC_000013.11:g.26252145_26252147del, NC_000013.11:g.26252146_26252147del, NC_000013.11:g.26252147del, NC_000013.11:g.26252147dup, NC_000013.11:g.26252146_26252147dup, NC_000013.11:g.26252145_26252147dup, NC_000013.11:g.26252144_26252147dup, NC_000013.11:g.26252143_26252147dup, NC_000013.11:g.26252142_26252147dup, NC_000013.10:g.26826273_26826284del, NC_000013.10:g.26826275_26826284del, NC_000013.10:g.26826276_26826284del, NC_000013.10:g.26826278_26826284del, NC_000013.10:g.26826279_26826284del, NC_000013.10:g.26826280_26826284del, NC_000013.10:g.26826281_26826284del, NC_000013.10:g.26826282_26826284del, NC_000013.10:g.26826283_26826284del, NC_000013.10:g.26826284del, NC_000013.10:g.26826284dup, NC_000013.10:g.26826283_26826284dup, NC_000013.10:g.26826282_26826284dup, NC_000013.10:g.26826281_26826284dup, NC_000013.10:g.26826280_26826284dup, NC_000013.10:g.26826279_26826284dup

Select item 14913197339.

rs1491319733 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 13:26329483 (GRCh38)
13:26903620 (GRCh37)
Canonical SPDI:: NC_000013.11:26329481:TGT:T
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000009/1 (GnomAD)
HGVS:: NC_000013.11:g.26329483_26329484del, NC_000013.10:g.26903620_26903621del

Select item 149130131910.

rs1491301319 has merged into rs1380947753 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGATGGATAGAT>-,GGATGGATAGATGGATGGATAGAT [Show Flanks]
Chromosome:: 13:26362262 (GRCh38)
13:26936399 (GRCh37)
Canonical SPDI:: NC_000013.11:26362258:GATGGATGGATAGAT:GAT,NC_000013.11:26362258:GATGGATGGATAGAT:GATGGATGGATAGATGGATGGATAGAT
Gene:: CDK8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GATGGATGGATAGATGGATGGATAGAT=0./0 (ALFA)
-=0.000315/44 (GnomAD)
HGVS:: NC_000013.11:g.26362262_26362273del, NC_000013.11:g.26362262_26362273dup, NC_000013.10:g.26936399_26936410del, NC_000013.10:g.26936399_26936410dup

Select item 149125598511.

rs1491255985 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:26309141 (GRCh38)
13:26883278 (GRCh37)
Canonical SPDI:: NC_000013.11:26309140:AT:
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00007/6 (GnomAD)
HGVS:: NC_000013.11:g.26309141_26309142del, NC_000013.10:g.26883278_26883279del

Select item 149124372512.

rs1491243725 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 13:26268256 (GRCh38)
13:26842393 (GRCh37)
Canonical SPDI:: NC_000013.11:26268255:AA:
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00068/11 (ALFA)
HGVS:: NC_000013.11:g.26268256_26268257del, NC_000013.10:g.26842393_26842394del

Select item 149124236713.

rs1491242367 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 13:26318058 (GRCh38)
13:26892195 (GRCh37)
Canonical SPDI:: NC_000013.11:26318055:AGAG:AG
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000023/6 (TOPMED)
HGVS:: NC_000013.11:g.26318056AG[1], NC_000013.10:g.26892193AG[1]

Select item 149122360314.

rs1491223603 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 13:26369710 (GRCh38)
13:26943848 (GRCh37)
Canonical SPDI:: NC_000013.11:26369710:TT:TTCTT
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTCTT=0.00017/2 (ALFA)
HGVS:: NC_000013.11:g.26369712_26369713insCTT, NC_000013.10:g.26943849_26943850insCTT

Select item 149121604415.

rs1491216044 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 13:26346173 (GRCh38)
13:26920310 (GRCh37)
Canonical SPDI:: NC_000013.11:26346172:CT:
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.26346173_26346174del, NC_000013.10:g.26920310_26920311del

Select item 149121030016.

rs1491210300 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 13:26388254 (GRCh38)
13:26962391 (GRCh37)
Canonical SPDI:: NC_000013.11:26388252:TAT:T
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.26388254_26388255del, NC_000013.10:g.26962391_26962392del

Select item 149120117017.

rs1491201170 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 13:26252125 (GRCh38)
13:26826262 (GRCh37)
Canonical SPDI:: NC_000013.11:26252124:CA:
Validated:: by frequency,by alfa
MAF:: -=0.00455/54 (ALFA)
-=0.00032/23 (GnomAD)
HGVS:: NC_000013.11:g.26252125_26252126del, NC_000013.10:g.26826262_26826263del

Select item 149117850918.

rs1491178509 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 13:26318056 (GRCh38)
13:26892194 (GRCh37)
Canonical SPDI:: NC_000013.11:26318056:G:GG
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.26318057dup, NC_000013.10:g.26892194dup

Select item 149116222719.

rs1491162227 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 13:26388253 (GRCh38)
13:26962391 (GRCh37)
Canonical SPDI:: NC_000013.11:26388253:A:AA
Gene:: CDK8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: A=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.26388254dup, NC_000013.10:g.26962391dup

Select item 149115532620.

rs1491155326 has merged into rs71188725 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 13:26363339 (GRCh38)
13:26937476 (GRCh37)
Canonical SPDI:: NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000013.11:26363327:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: CDK8 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000013.11:g.26363339_26363341del, NC_000013.11:g.26363340_26363341del, NC_000013.11:g.26363341del, NC_000013.11:g.26363341dup, NC_000013.11:g.26363340_26363341dup, NC_000013.11:g.26363339_26363341dup, NC_000013.11:g.26363338_26363341dup, NC_000013.11:g.26363337_26363341dup, NC_000013.11:g.26363336_26363341dup, NC_000013.11:g.26363335_26363341dup, NC_000013.11:g.26363334_26363341dup, NC_000013.11:g.26363333_26363341dup, NC_000013.11:g.26363332_26363341dup, NC_000013.11:g.26363331_26363341dup, NC_000013.11:g.26363330_26363341dup, NC_000013.11:g.26363329_26363341dup, NC_000013.11:g.26363328_26363341dup, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.11:g.26363341_26363342insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.26937476_26937478del, NC_000013.10:g.26937477_26937478del, NC_000013.10:g.26937478del, NC_000013.10:g.26937478dup, NC_000013.10:g.26937477_26937478dup, NC_000013.10:g.26937476_26937478dup, NC_000013.10:g.26937475_26937478dup, NC_000013.10:g.26937474_26937478dup, NC_000013.10:g.26937473_26937478dup, NC_000013.10:g.26937472_26937478dup, NC_000013.10:g.26937471_26937478dup, NC_000013.10:g.26937470_26937478dup, NC_000013.10:g.26937469_26937478dup, NC_000013.10:g.26937468_26937478dup, NC_000013.10:g.26937467_26937478dup, NC_000013.10:g.26937466_26937478dup, NC_000013.10:g.26937465_26937478dup, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAA, NC_000013.10:g.26937478_26937479insAAAAAAAAAAAAAAAAAAAAAAAAA

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