SNP Links for Gene (Select 84433) - SNP

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Select item 14915793681.

rs1491579368 has merged into rs898113665 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 7:3018181 (GRCh38)
7:3057815 (GRCh37)
Canonical SPDI:: NC_000007.14:3018169:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000007.14:3018169:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:3018169:TTTTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.3018181_3018182del, NC_000007.14:g.3018182del, NC_000007.14:g.3018182dup, NC_000007.13:g.3057815_3057816del, NC_000007.13:g.3057816del, NC_000007.13:g.3057816dup, NG_027759.1:g.30705_30706del, NG_027759.1:g.30706del, NG_027759.1:g.30706dup

Select item 14915766962.

rs1491576696 has merged into rs774800628 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 7:2933708 (GRCh38)
7:2973342 (GRCh37)
Canonical SPDI:: NC_000007.14:2933706:TCT:T,NC_000007.14:2933706:TCT:TCTCT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
-=0.00032/7 (TOMMO)
-=0.0062/23 (TWINSUK)
-=0.0083/32 (ALSPAC)
HGVS:: NC_000007.14:g.2933708_2933709del, NC_000007.14:g.2933708_2933709dup, NC_000007.13:g.2973342_2973343del, NC_000007.13:g.2973342_2973343dup, NG_027759.1:g.115168_115169del, NG_027759.1:g.115168_115169dup

Select item 14915430683.

rs1491543068 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT,CTTTCCTT,CTTTCTT,CTTTCTTTCTT,CTTTCTTTCTTTCTT [Show Flanks]
Chromosome:: 7:2933721 (GRCh38)
7:2973356 (GRCh37)
Canonical SPDI:: NC_000007.14:2933721:TT:TTCTT,NC_000007.14:2933721:TT:TTCTTTCCTT,NC_000007.14:2933721:TT:TTCTTTCTT,NC_000007.14:2933721:TT:TTCTTTCTTTCTT,NC_000007.14:2933721:TT:TTCTTTCTTTCTTTCTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTTTCCTT=0./0 (ALFA)
TTCTTTCC=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.2933723_2933724insCTT, NC_000007.14:g.2933723_2933724insCTTTCCTT, NC_000007.14:g.2933722_2933723TTCT[2]T[1], NC_000007.14:g.2933722_2933723TTCT[3]T[1], NC_000007.14:g.2933722_2933723TTCT[4]T[1], NC_000007.13:g.2973357_2973358insCTT, NC_000007.13:g.2973357_2973358insCTTTCCTT, NC_000007.13:g.2973356_2973357TTCT[2]T[1], NC_000007.13:g.2973356_2973357TTCT[3]T[1], NC_000007.13:g.2973356_2973357TTCT[4]T[1], NG_027759.1:g.115154_115155insGAA, NG_027759.1:g.115154_115155insGGAAAGAA, NG_027759.1:g.115153_115154AAGA[2]A[1], NG_027759.1:g.115153_115154AAGA[3]A[1], NG_027759.1:g.115153_115154AAGA[4]A[1]

Select item 14915283504.

rs1491528350 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 7:3023583 (GRCh38)
7:3063217 (GRCh37)
Canonical SPDI:: NC_000007.14:3023581:TCT:T
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000007.14:g.3023583_3023584del, NC_000007.13:g.3063217_3063218del, NG_027759.1:g.25293_25294del

Select item 14915193985.

rs1491519398 has merged into rs869031657 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:3040353 (GRCh38)
7:3079987 (GRCh37)
Canonical SPDI:: NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3040345:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.3040353_3040361del, NC_000007.14:g.3040358_3040361del, NC_000007.14:g.3040359_3040361del, NC_000007.14:g.3040360_3040361del, NC_000007.14:g.3040361del, NC_000007.14:g.3040361dup, NC_000007.14:g.3040360_3040361dup, NC_000007.14:g.3040359_3040361dup, NC_000007.14:g.3040358_3040361dup, NC_000007.14:g.3040357_3040361dup, NC_000007.14:g.3040355_3040361dup, NC_000007.14:g.3040353_3040361dup, NC_000007.14:g.3040352_3040361dup, NC_000007.14:g.3040351_3040361dup, NC_000007.14:g.3040350_3040361dup, NC_000007.14:g.3040349_3040361dup, NC_000007.14:g.3040361_3040362insTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.3040361_3040362insTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.3040361_3040362insTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.3079987_3079995del, NC_000007.13:g.3079992_3079995del, NC_000007.13:g.3079993_3079995del, NC_000007.13:g.3079994_3079995del, NC_000007.13:g.3079995del, NC_000007.13:g.3079995dup, NC_000007.13:g.3079994_3079995dup, NC_000007.13:g.3079993_3079995dup, NC_000007.13:g.3079992_3079995dup, NC_000007.13:g.3079991_3079995dup, NC_000007.13:g.3079989_3079995dup, NC_000007.13:g.3079987_3079995dup, NC_000007.13:g.3079986_3079995dup, NC_000007.13:g.3079985_3079995dup, NC_000007.13:g.3079984_3079995dup, NC_000007.13:g.3079983_3079995dup, NC_000007.13:g.3079995_3079996insTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.3079995_3079996insTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.3079995_3079996insTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.8522_8530del, NG_027759.1:g.8527_8530del, NG_027759.1:g.8528_8530del, NG_027759.1:g.8529_8530del, NG_027759.1:g.8530del, NG_027759.1:g.8530dup, NG_027759.1:g.8529_8530dup, NG_027759.1:g.8528_8530dup, NG_027759.1:g.8527_8530dup, NG_027759.1:g.8526_8530dup, NG_027759.1:g.8524_8530dup, NG_027759.1:g.8522_8530dup, NG_027759.1:g.8521_8530dup, NG_027759.1:g.8520_8530dup, NG_027759.1:g.8519_8530dup, NG_027759.1:g.8518_8530dup, NG_027759.1:g.8530_8531insAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.8530_8531insAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.8530_8531insAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915182876.

rs1491518287 [Homo sapiens]

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

Select item 14915153087.

rs1491515308 has merged into rs34011596 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:3036060 (GRCh38)
7:3075694 (GRCh37)
Canonical SPDI:: NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:3036045:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.1969/986 (1000Genomes)
HGVS:: NC_000007.14:g.3036060_3036064del, NC_000007.14:g.3036061_3036064del, NC_000007.14:g.3036062_3036064del, NC_000007.14:g.3036063_3036064del, NC_000007.14:g.3036064del, NC_000007.14:g.3036064dup, NC_000007.14:g.3036063_3036064dup, NC_000007.14:g.3036062_3036064dup, NC_000007.14:g.3036052_3036064dup, NC_000007.13:g.3075694_3075698del, NC_000007.13:g.3075695_3075698del, NC_000007.13:g.3075696_3075698del, NC_000007.13:g.3075697_3075698del, NC_000007.13:g.3075698del, NC_000007.13:g.3075698dup, NC_000007.13:g.3075697_3075698dup, NC_000007.13:g.3075696_3075698dup, NC_000007.13:g.3075686_3075698dup, NG_027759.1:g.12826_12830del, NG_027759.1:g.12827_12830del, NG_027759.1:g.12828_12830del, NG_027759.1:g.12829_12830del, NG_027759.1:g.12830del, NG_027759.1:g.12830dup, NG_027759.1:g.12829_12830dup, NG_027759.1:g.12828_12830dup, NG_027759.1:g.12818_12830dup

Select item 14915065308.

rs1491506530 has merged into rs3839716 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA [Show Flanks]
Chromosome:: 7:2945741 (GRCh38)
7:2985375 (GRCh37)
Canonical SPDI:: NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000007.14:2945727:ACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA
Gene:: CARD11 (Varview), CARD11-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACACACA=0./0 (ALFA)
-=0.0929/358 (ALSPAC)
AC=0.3883/233 (NorthernSweden)
HGVS:: NC_000007.14:g.2945729CA[6], NC_000007.14:g.2945729CA[7], NC_000007.14:g.2945729CA[8], NC_000007.14:g.2945729CA[9], NC_000007.14:g.2945729CA[10], NC_000007.14:g.2945729CA[11], NC_000007.14:g.2945729CA[12], NC_000007.14:g.2945729CA[14], NC_000007.14:g.2945729CA[15], NC_000007.14:g.2945729CA[16], NC_000007.14:g.2945729CA[17], NC_000007.13:g.2985363CA[6], NC_000007.13:g.2985363CA[7], NC_000007.13:g.2985363CA[8], NC_000007.13:g.2985363CA[9], NC_000007.13:g.2985363CA[10], NC_000007.13:g.2985363CA[11], NC_000007.13:g.2985363CA[12], NC_000007.13:g.2985363CA[14], NC_000007.13:g.2985363CA[15], NC_000007.13:g.2985363CA[16], NC_000007.13:g.2985363CA[17], NG_027759.1:g.103123GT[6], NG_027759.1:g.103123GT[7], NG_027759.1:g.103123GT[8], NG_027759.1:g.103123GT[9], NG_027759.1:g.103123GT[10], NG_027759.1:g.103123GT[11], NG_027759.1:g.103123GT[12], NG_027759.1:g.103123GT[14], NG_027759.1:g.103123GT[15], NG_027759.1:g.103123GT[16], NG_027759.1:g.103123GT[17]

Select item 14915031139.

rs1491503113 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 7:2933684 (GRCh38)
7:2973318 (GRCh37)
Canonical SPDI:: NC_000007.14:2933682:TCT:T
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
-=0.00098/70 (GnomAD)
HGVS:: NC_000007.14:g.2933684_2933685del, NC_000007.13:g.2973318_2973319del, NG_027759.1:g.115192_115193del

Select item 149148391810.

rs1491483918 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:2976881 (GRCh38)
7:3016515 (GRCh37)
Canonical SPDI:: NC_000007.14:2976880:CA:
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000007.14:g.2976881_2976882del, NC_000007.13:g.3016515_3016516del, NG_027759.1:g.71994_71995del

Select item 149148052311.

rs1491480523 has merged into rs1185500862 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:2957648 (GRCh38)
7:2997282 (GRCh37)
Canonical SPDI:: NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2957637:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.2957648_2957659del, NC_000007.14:g.2957651_2957659del, NC_000007.14:g.2957652_2957659del, NC_000007.14:g.2957653_2957659del, NC_000007.14:g.2957654_2957659del, NC_000007.14:g.2957655_2957659del, NC_000007.14:g.2957656_2957659del, NC_000007.14:g.2957657_2957659del, NC_000007.14:g.2957658_2957659del, NC_000007.14:g.2957659del, NC_000007.14:g.2957659dup, NC_000007.14:g.2957658_2957659dup, NC_000007.14:g.2957657_2957659dup, NC_000007.14:g.2957656_2957659dup, NC_000007.14:g.2957655_2957659dup, NC_000007.14:g.2957652_2957659dup, NC_000007.13:g.2997282_2997293del, NC_000007.13:g.2997285_2997293del, NC_000007.13:g.2997286_2997293del, NC_000007.13:g.2997287_2997293del, NC_000007.13:g.2997288_2997293del, NC_000007.13:g.2997289_2997293del, NC_000007.13:g.2997290_2997293del, NC_000007.13:g.2997291_2997293del, NC_000007.13:g.2997292_2997293del, NC_000007.13:g.2997293del, NC_000007.13:g.2997293dup, NC_000007.13:g.2997292_2997293dup, NC_000007.13:g.2997291_2997293dup, NC_000007.13:g.2997290_2997293dup, NC_000007.13:g.2997289_2997293dup, NC_000007.13:g.2997286_2997293dup, NG_027759.1:g.91227_91238del, NG_027759.1:g.91230_91238del, NG_027759.1:g.91231_91238del, NG_027759.1:g.91232_91238del, NG_027759.1:g.91233_91238del, NG_027759.1:g.91234_91238del, NG_027759.1:g.91235_91238del, NG_027759.1:g.91236_91238del, NG_027759.1:g.91237_91238del, NG_027759.1:g.91238del, NG_027759.1:g.91238dup, NG_027759.1:g.91237_91238dup, NG_027759.1:g.91236_91238dup, NG_027759.1:g.91235_91238dup, NG_027759.1:g.91234_91238dup, NG_027759.1:g.91231_91238dup

Select item 149147422412.

rs1491474224 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTT [Show Flanks]
Chromosome:: 7:3040346 (GRCh38)
7:3079981 (GRCh37)
Canonical SPDI:: NC_000007.14:3040346:TT:TTGTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTGTT=0./0 (ALFA)
TTG=0.00016/11 (GnomAD)
HGVS:: NC_000007.14:g.3040348_3040349insGTT, NC_000007.13:g.3079982_3079983insGTT, NG_027759.1:g.8529_8530insCAA

Select item 149143617013.

rs1491436170 has merged into rs1000624314 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:2933316 (GRCh38)
7:2972950 (GRCh37)
Canonical SPDI:: NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:2933306:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.2933316_2933330del, NC_000007.14:g.2933320_2933330del, NC_000007.14:g.2933321_2933330del, NC_000007.14:g.2933322_2933330del, NC_000007.14:g.2933323_2933330del, NC_000007.14:g.2933324_2933330del, NC_000007.14:g.2933325_2933330del, NC_000007.14:g.2933326_2933330del, NC_000007.14:g.2933327_2933330del, NC_000007.14:g.2933328_2933330del, NC_000007.14:g.2933329_2933330del, NC_000007.14:g.2933330del, NC_000007.14:g.2933330dup, NC_000007.14:g.2933329_2933330dup, NC_000007.14:g.2933328_2933330dup, NC_000007.14:g.2933327_2933330dup, NC_000007.14:g.2933326_2933330dup, NC_000007.14:g.2933325_2933330dup, NC_000007.14:g.2933324_2933330dup, NC_000007.14:g.2933323_2933330dup, NC_000007.14:g.2933322_2933330dup, NC_000007.14:g.2933321_2933330dup, NC_000007.14:g.2933320_2933330dup, NC_000007.14:g.2933316_2933330dup, NC_000007.14:g.2933310_2933330dup, NC_000007.14:g.2933308_2933330dup, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.14:g.2933330_2933331insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972950_2972964del, NC_000007.13:g.2972954_2972964del, NC_000007.13:g.2972955_2972964del, NC_000007.13:g.2972956_2972964del, NC_000007.13:g.2972957_2972964del, NC_000007.13:g.2972958_2972964del, NC_000007.13:g.2972959_2972964del, NC_000007.13:g.2972960_2972964del, NC_000007.13:g.2972961_2972964del, NC_000007.13:g.2972962_2972964del, NC_000007.13:g.2972963_2972964del, NC_000007.13:g.2972964del, NC_000007.13:g.2972964dup, NC_000007.13:g.2972963_2972964dup, NC_000007.13:g.2972962_2972964dup, NC_000007.13:g.2972961_2972964dup, NC_000007.13:g.2972960_2972964dup, NC_000007.13:g.2972959_2972964dup, NC_000007.13:g.2972958_2972964dup, NC_000007.13:g.2972957_2972964dup, NC_000007.13:g.2972956_2972964dup, NC_000007.13:g.2972955_2972964dup, NC_000007.13:g.2972954_2972964dup, NC_000007.13:g.2972950_2972964dup, NC_000007.13:g.2972944_2972964dup, NC_000007.13:g.2972942_2972964dup, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.2972964_2972965insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.115555_115569del, NG_027759.1:g.115559_115569del, NG_027759.1:g.115560_115569del, NG_027759.1:g.115561_115569del, NG_027759.1:g.115562_115569del, NG_027759.1:g.115563_115569del, NG_027759.1:g.115564_115569del, NG_027759.1:g.115565_115569del, NG_027759.1:g.115566_115569del, NG_027759.1:g.115567_115569del, NG_027759.1:g.115568_115569del, NG_027759.1:g.115569del, NG_027759.1:g.115569dup, NG_027759.1:g.115568_115569dup, NG_027759.1:g.115567_115569dup, NG_027759.1:g.115566_115569dup, NG_027759.1:g.115565_115569dup, NG_027759.1:g.115564_115569dup, NG_027759.1:g.115563_115569dup, NG_027759.1:g.115562_115569dup, NG_027759.1:g.115561_115569dup, NG_027759.1:g.115560_115569dup, NG_027759.1:g.115559_115569dup, NG_027759.1:g.115555_115569dup, NG_027759.1:g.115549_115569dup, NG_027759.1:g.115547_115569dup, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.115569_115570insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149141673914.

rs1491416739 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 7:3036045 (GRCh38)
7:3075679 (GRCh37)
Canonical SPDI:: NC_000007.14:3036044:AT:
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00006/5 (GnomAD)
HGVS:: NC_000007.14:g.3036045_3036046del, NC_000007.13:g.3075679_3075680del, NG_027759.1:g.12830_12831del

Select item 149141304115.

rs1491413041 has merged into rs1463930216 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 7:2933704 (GRCh38)
7:2973338 (GRCh37)
Canonical SPDI:: NC_000007.14:2933702:TCT:T,NC_000007.14:2933702:TCT:TCTCT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
-=0.00006/4 (GnomAD)
HGVS:: NC_000007.14:g.2933704_2933705del, NC_000007.14:g.2933704_2933705dup, NC_000007.13:g.2973338_2973339del, NC_000007.13:g.2973338_2973339dup, NG_027759.1:g.115172_115173del, NG_027759.1:g.115172_115173dup

Select item 149140682116.

rs1491406821 has merged into rs869179009 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAAA>-,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 7:2943756 (GRCh38)
7:2983390 (GRCh37)
Canonical SPDI:: NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:2943748:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: CARD11 (Varview), CARD11-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAA=0./0 (ALFA)
HGVS:: NC_000007.14:g.2943756_2943778del, NC_000007.14:g.2943761_2943778del, NC_000007.14:g.2943762_2943778del, NC_000007.14:g.2943764_2943778del, NC_000007.14:g.2943765_2943778del, NC_000007.14:g.2943766_2943778del, NC_000007.14:g.2943767_2943778del, NC_000007.14:g.2943768_2943778del, NC_000007.14:g.2943769_2943778del, NC_000007.14:g.2943770_2943778del, NC_000007.14:g.2943771_2943778del, NC_000007.14:g.2943772_2943778del, NC_000007.14:g.2943773_2943778del, NC_000007.14:g.2943774_2943778del, NC_000007.14:g.2943775_2943778del, NC_000007.14:g.2943776_2943778del, NC_000007.14:g.2943777_2943778del, NC_000007.14:g.2943778del, NC_000007.14:g.2943778dup, NC_000007.14:g.2943777_2943778dup, NC_000007.14:g.2943776_2943778dup, NC_000007.14:g.2943775_2943778dup, NC_000007.14:g.2943774_2943778dup, NC_000007.14:g.2943773_2943778dup, NC_000007.14:g.2943772_2943778dup, NC_000007.14:g.2943771_2943778dup, NC_000007.14:g.2943770_2943778dup, NC_000007.14:g.2943769_2943778dup, NC_000007.14:g.2943768_2943778dup, NC_000007.14:g.2943767_2943778dup, NC_000007.14:g.2943766_2943778dup, NC_000007.14:g.2943765_2943778dup, NC_000007.14:g.2943764_2943778dup, NC_000007.14:g.2943763_2943778dup, NC_000007.14:g.2943762_2943778dup, NC_000007.14:g.2943761_2943778dup, NC_000007.14:g.2943760_2943778dup, NC_000007.14:g.2943759_2943778dup, NC_000007.14:g.2943758_2943778dup, NC_000007.14:g.2943757_2943778dup, NC_000007.14:g.2943756_2943778dup, NC_000007.14:g.2943755_2943778dup, NC_000007.14:g.2943754_2943778dup, NC_000007.14:g.2943753_2943778dup, NC_000007.14:g.2943752_2943778dup, NC_000007.14:g.2943751_2943778dup, NC_000007.14:g.2943749_2943778dup, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.14:g.2943778_2943779insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983390_2983412del, NC_000007.13:g.2983395_2983412del, NC_000007.13:g.2983396_2983412del, NC_000007.13:g.2983398_2983412del, NC_000007.13:g.2983399_2983412del, NC_000007.13:g.2983400_2983412del, NC_000007.13:g.2983401_2983412del, NC_000007.13:g.2983402_2983412del, NC_000007.13:g.2983403_2983412del, NC_000007.13:g.2983404_2983412del, NC_000007.13:g.2983405_2983412del, NC_000007.13:g.2983406_2983412del, NC_000007.13:g.2983407_2983412del, NC_000007.13:g.2983408_2983412del, NC_000007.13:g.2983409_2983412del, NC_000007.13:g.2983410_2983412del, NC_000007.13:g.2983411_2983412del, NC_000007.13:g.2983412del, NC_000007.13:g.2983412dup, NC_000007.13:g.2983411_2983412dup, NC_000007.13:g.2983410_2983412dup, NC_000007.13:g.2983409_2983412dup, NC_000007.13:g.2983408_2983412dup, NC_000007.13:g.2983407_2983412dup, NC_000007.13:g.2983406_2983412dup, NC_000007.13:g.2983405_2983412dup, NC_000007.13:g.2983404_2983412dup, NC_000007.13:g.2983403_2983412dup, NC_000007.13:g.2983402_2983412dup, NC_000007.13:g.2983401_2983412dup, NC_000007.13:g.2983400_2983412dup, NC_000007.13:g.2983399_2983412dup, NC_000007.13:g.2983398_2983412dup, NC_000007.13:g.2983397_2983412dup, NC_000007.13:g.2983396_2983412dup, NC_000007.13:g.2983395_2983412dup, NC_000007.13:g.2983394_2983412dup, NC_000007.13:g.2983393_2983412dup, NC_000007.13:g.2983392_2983412dup, NC_000007.13:g.2983391_2983412dup, NC_000007.13:g.2983390_2983412dup, NC_000007.13:g.2983389_2983412dup, NC_000007.13:g.2983388_2983412dup, NC_000007.13:g.2983387_2983412dup, NC_000007.13:g.2983386_2983412dup, NC_000007.13:g.2983385_2983412dup, NC_000007.13:g.2983383_2983412dup, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000007.13:g.2983412_2983413insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_027759.1:g.105105_105127del, NG_027759.1:g.105110_105127del, NG_027759.1:g.105111_105127del, NG_027759.1:g.105113_105127del, NG_027759.1:g.105114_105127del, NG_027759.1:g.105115_105127del, NG_027759.1:g.105116_105127del, NG_027759.1:g.105117_105127del, NG_027759.1:g.105118_105127del, NG_027759.1:g.105119_105127del, NG_027759.1:g.105120_105127del, NG_027759.1:g.105121_105127del, NG_027759.1:g.105122_105127del, NG_027759.1:g.105123_105127del, NG_027759.1:g.105124_105127del, NG_027759.1:g.105125_105127del, NG_027759.1:g.105126_105127del, NG_027759.1:g.105127del, NG_027759.1:g.105127dup, NG_027759.1:g.105126_105127dup, NG_027759.1:g.105125_105127dup, NG_027759.1:g.105124_105127dup, NG_027759.1:g.105123_105127dup, NG_027759.1:g.105122_105127dup, NG_027759.1:g.105121_105127dup, NG_027759.1:g.105120_105127dup, NG_027759.1:g.105119_105127dup, NG_027759.1:g.105118_105127dup, NG_027759.1:g.105117_105127dup, NG_027759.1:g.105116_105127dup, NG_027759.1:g.105115_105127dup, NG_027759.1:g.105114_105127dup, NG_027759.1:g.105113_105127dup, NG_027759.1:g.105112_105127dup, NG_027759.1:g.105111_105127dup, NG_027759.1:g.105110_105127dup, NG_027759.1:g.105109_105127dup, NG_027759.1:g.105108_105127dup, NG_027759.1:g.105107_105127dup, NG_027759.1:g.105106_105127dup, NG_027759.1:g.105105_105127dup, NG_027759.1:g.105104_105127dup, NG_027759.1:g.105103_105127dup, NG_027759.1:g.105102_105127dup, NG_027759.1:g.105101_105127dup, NG_027759.1:g.105100_105127dup, NG_027759.1:g.105098_105127dup, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_027759.1:g.105127_105128insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149140239617.

rs1491402396 has merged into rs71029603 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA [Show Flanks]
Chromosome:: 7:3022932 (GRCh38)
7:3062566 (GRCh37)
Canonical SPDI:: NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:3022919:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.20141/114 (NorthernSweden)
-=0.475/19 (GENOME_DK)
HGVS:: NC_000007.14:g.3022932_3022936del, NC_000007.14:g.3022933_3022936del, NC_000007.14:g.3022934_3022936del, NC_000007.14:g.3022935_3022936del, NC_000007.14:g.3022936del, NC_000007.14:g.3022936dup, NC_000007.14:g.3022935_3022936dup, NC_000007.13:g.3062566_3062570del, NC_000007.13:g.3062567_3062570del, NC_000007.13:g.3062568_3062570del, NC_000007.13:g.3062569_3062570del, NC_000007.13:g.3062570del, NC_000007.13:g.3062570dup, NC_000007.13:g.3062569_3062570dup, NG_027759.1:g.25952_25956del, NG_027759.1:g.25953_25956del, NG_027759.1:g.25954_25956del, NG_027759.1:g.25955_25956del, NG_027759.1:g.25956del, NG_027759.1:g.25956dup, NG_027759.1:g.25955_25956dup

Select item 149139640818.

rs1491396408 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 7:2933692 (GRCh38)
7:2973326 (GRCh37)
Canonical SPDI:: NC_000007.14:2933690:TCT:T,NC_000007.14:2933690:TCT:TCTCT
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
HGVS:: NC_000007.14:g.2933692_2933693del, NC_000007.14:g.2933692_2933693dup, NC_000007.13:g.2973326_2973327del, NC_000007.13:g.2973326_2973327dup, NG_027759.1:g.115184_115185del, NG_027759.1:g.115184_115185dup

Select item 149139200919.

rs1491392009 has merged into rs112208244 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACA>-,CA,CACACA [Show Flanks]
Chromosome:: 7:2935025 (GRCh38)
7:2974659 (GRCh37)
Canonical SPDI:: NC_000007.14:2935015:ACACACACACACA:ACACACACA,NC_000007.14:2935015:ACACACACACACA:ACACACACACA,NC_000007.14:2935015:ACACACACACACA:ACACACACACACACA
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACACACA=0./0 (ALFA)
-=0.150909/83 (NorthernSweden)
-=0.18559/340 (Korea1K)
-=0.188299/943 (1000Genomes)
-=0.193203/51139 (TOPMED)
-=0.194069/3251 (TOMMO)
-=0.359493/1333 (TWINSUK)
-=0.364297/1404 (ALSPAC)
HGVS:: NC_000007.14:g.2935017CA[4], NC_000007.14:g.2935017CA[5], NC_000007.14:g.2935017CA[7], NC_000007.13:g.2974651CA[4], NC_000007.13:g.2974651CA[5], NC_000007.13:g.2974651CA[7], NG_027759.1:g.113849GT[4], NG_027759.1:g.113849GT[5], NG_027759.1:g.113849GT[7]

Select item 149139050620.

rs1491390506 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:3027956 (GRCh38)
7:3067590 (GRCh37)
Canonical SPDI:: NC_000007.14:3027955:CA:
Gene:: CARD11 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00337/40 (ALFA)
-=0.00042/11 (TOMMO)
HGVS:: NC_000007.14:g.3027956_3027957del, NC_000007.13:g.3067590_3067591del, NG_027759.1:g.20919_20920del

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