SNP Links for Gene (Select 9531) - SNP

Links from Gene

Items: 1 to 20 of 7502

<< First< Prev

Page of 376

Next >Last >>

Select item 14915092901.

rs1491509290 has merged into rs1161102936 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:119665154 (GRCh38)
10:121424666 (GRCh37)
Canonical SPDI:: NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119665144:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.119665154_119665155del, NC_000010.11:g.119665155del, NC_000010.11:g.119665155dup, NC_000010.11:g.119665154_119665155dup, NC_000010.11:g.119665153_119665155dup, NC_000010.11:g.119665152_119665155dup, NC_000010.11:g.119665151_119665155dup, NC_000010.11:g.119665150_119665155dup, NC_000010.11:g.119665149_119665155dup, NC_000010.11:g.119665148_119665155dup, NC_000010.11:g.119665147_119665155dup, NC_000010.11:g.119665146_119665155dup, NC_000010.11:g.119665145_119665155dup, NC_000010.10:g.121424666_121424667del, NC_000010.10:g.121424667del, NC_000010.10:g.121424667dup, NC_000010.10:g.121424666_121424667dup, NC_000010.10:g.121424665_121424667dup, NC_000010.10:g.121424664_121424667dup, NC_000010.10:g.121424663_121424667dup, NC_000010.10:g.121424662_121424667dup, NC_000010.10:g.121424661_121424667dup, NC_000010.10:g.121424660_121424667dup, NC_000010.10:g.121424659_121424667dup, NC_000010.10:g.121424658_121424667dup, NC_000010.10:g.121424657_121424667dup, NG_016125.1:g.18785_18786del, NG_016125.1:g.18786del, NG_016125.1:g.18786dup, NG_016125.1:g.18785_18786dup, NG_016125.1:g.18784_18786dup, NG_016125.1:g.18783_18786dup, NG_016125.1:g.18782_18786dup, NG_016125.1:g.18781_18786dup, NG_016125.1:g.18780_18786dup, NG_016125.1:g.18779_18786dup, NG_016125.1:g.18778_18786dup, NG_016125.1:g.18777_18786dup, NG_016125.1:g.18776_18786dup

Select item 14914886282.

rs1491488628 [Homo sapiens]

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

Select item 14914305443.

rs1491430544 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,CC [Show Flanks]
Chromosome:: 10:119665145 (GRCh38)
10:121424658 (GRCh37)
Canonical SPDI:: NC_000010.11:119665145::A,NC_000010.11:119665145::ATA,NC_000010.11:119665145::ATATA,NC_000010.11:119665145::CC
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
A=0.00057/1 (Korea1K)
A=0.00174/27 (TOMMO)
HGVS:: NC_000010.11:g.119665145_119665146insA, NC_000010.11:g.119665145_119665146insATA, NC_000010.11:g.119665145_119665146insATATA, NC_000010.11:g.119665145_119665146insCC, NC_000010.10:g.121424657_121424658insA, NC_000010.10:g.121424657_121424658insATA, NC_000010.10:g.121424657_121424658insATATA, NC_000010.10:g.121424657_121424658insCC, NG_016125.1:g.18776_18777insA, NG_016125.1:g.18776_18777insATA, NG_016125.1:g.18776_18777insATATA, NG_016125.1:g.18776_18777insCC

Select item 14914305174.

rs1491430517 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTCC [Show Flanks]
Chromosome:: 10:119675882 (GRCh38)
10:121435395 (GRCh37)
Canonical SPDI:: NC_000010.11:119675882:TCC:TCCCTCC
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCCCTCC=0./0 (ALFA)
TCCC=0.00083/11 (TOMMO)
HGVS:: NC_000010.11:g.119675885_119675886insCTCC, NC_000010.10:g.121435397_121435398insCTCC, NG_016125.1:g.29516_29517insCTCC

Select item 14914110805.

rs1491411080 [Homo sapiens]

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

Select item 14913443426.

rs1491344342 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: 10:119665140 (GRCh38)
10:121424653 (GRCh37)
Canonical SPDI:: NC_000010.11:119665140:T:TT,NC_000010.11:119665140:T:TTTT,NC_000010.11:119665140:T:TTTTT,NC_000010.11:119665140:T:TTTTTT,NC_000010.11:119665140:T:TTTTTTT,NC_000010.11:119665140:T:TTTTTTTT,NC_000010.11:119665140:T:TTTTTTTTT,NC_000010.11:119665140:T:TTTTTTTTTT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
TTTTTT=0.00115/18 (TOMMO)
HGVS:: NC_000010.11:g.119665141dup, NC_000010.11:g.119665141_119665142insTTT, NC_000010.11:g.119665141_119665142insTTTT, NC_000010.11:g.119665141_119665142insTTTTT, NC_000010.11:g.119665141_119665142insTTTTTT, NC_000010.11:g.119665141_119665142insTTTTTTT, NC_000010.11:g.119665141_119665142insTTTTTTTT, NC_000010.11:g.119665141_119665142insTTTTTTTTT, NC_000010.10:g.121424653dup, NC_000010.10:g.121424653_121424654insTTT, NC_000010.10:g.121424653_121424654insTTTT, NC_000010.10:g.121424653_121424654insTTTTT, NC_000010.10:g.121424653_121424654insTTTTTT, NC_000010.10:g.121424653_121424654insTTTTTTT, NC_000010.10:g.121424653_121424654insTTTTTTTT, NC_000010.10:g.121424653_121424654insTTTTTTTTT, NG_016125.1:g.18772dup, NG_016125.1:g.18772_18773insTTT, NG_016125.1:g.18772_18773insTTTT, NG_016125.1:g.18772_18773insTTTTT, NG_016125.1:g.18772_18773insTTTTTT, NG_016125.1:g.18772_18773insTTTTTTT, NG_016125.1:g.18772_18773insTTTTTTTT, NG_016125.1:g.18772_18773insTTTTTTTTT

Select item 14913305947.

rs1491330594 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>-,CCC,CCCC [Show Flanks]
Chromosome:: 10:119675800 (GRCh38)
10:121435312 (GRCh37)
Canonical SPDI:: NC_000010.11:119675797:CCCC:CC,NC_000010.11:119675797:CCCC:CCCCC,NC_000010.11:119675797:CCCC:CCCCCC
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCC=0./0 (ALFA)
-=0.0002/4 (TOMMO)
HGVS:: NC_000010.11:g.119675800_119675801del, NC_000010.11:g.119675801dup, NC_000010.11:g.119675800_119675801dup, NC_000010.10:g.121435312_121435313del, NC_000010.10:g.121435313dup, NC_000010.10:g.121435312_121435313dup, NG_016125.1:g.29431_29432del, NG_016125.1:g.29432dup, NG_016125.1:g.29431_29432dup

Select item 14912607118.

rs1491260711 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 10:119675797 (GRCh38)
10:121435309 (GRCh37)
Canonical SPDI:: NC_000010.11:119675796:TC:
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01307/155 (ALFA)
-=0.00341/46 (TOMMO)
-=0.00473/8 (Korea1K)
-=0.02098/12 (NorthernSweden)
HGVS:: NC_000010.11:g.119675797_119675798del, NC_000010.10:g.121435309_121435310del, NG_016125.1:g.29428_29429del

Select item 14911025219.

rs1491102521 [Homo sapiens]

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

Select item 149108169910.

rs1491081699 has merged into rs1554876557 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGTGTGTGTGTGTGTGT>-,GT,GTGT,GTGTGTGT,GTGTGTGTGT,GTGTGTGTGTGT,GTGTGTGTGTGTGT,GTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT [Show Flanks]
Chromosome:: 10:119665108 (GRCh38)
10:121424620 (GRCh37)
Canonical SPDI:: NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT,NC_000010.11:119665092:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT:TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGTGTGT=0./0 (ALFA)
TG=0.04694/775 (TOMMO)
HGVS:: NC_000010.11:g.119665094GT[7], NC_000010.11:g.119665094GT[8], NC_000010.11:g.119665094GT[9], NC_000010.11:g.119665094GT[11], NC_000010.11:g.119665094GT[12], NC_000010.11:g.119665094GT[13], NC_000010.11:g.119665094GT[14], NC_000010.11:g.119665094GT[15], NC_000010.11:g.119665094GT[16], NC_000010.11:g.119665094GT[18], NC_000010.11:g.119665094GT[19], NC_000010.11:g.119665094GT[20], NC_000010.11:g.119665094GT[21], NC_000010.11:g.119665094GT[22], NC_000010.11:g.119665094GT[23], NC_000010.11:g.119665094GT[24], NC_000010.11:g.119665094GT[25], NC_000010.10:g.121424606GT[7], NC_000010.10:g.121424606GT[8], NC_000010.10:g.121424606GT[9], NC_000010.10:g.121424606GT[11], NC_000010.10:g.121424606GT[12], NC_000010.10:g.121424606GT[13], NC_000010.10:g.121424606GT[14], NC_000010.10:g.121424606GT[15], NC_000010.10:g.121424606GT[16], NC_000010.10:g.121424606GT[18], NC_000010.10:g.121424606GT[19], NC_000010.10:g.121424606GT[20], NC_000010.10:g.121424606GT[21], NC_000010.10:g.121424606GT[22], NC_000010.10:g.121424606GT[23], NC_000010.10:g.121424606GT[24], NC_000010.10:g.121424606GT[25], NG_016125.1:g.18725GT[7], NG_016125.1:g.18725GT[8], NG_016125.1:g.18725GT[9], NG_016125.1:g.18725GT[11], NG_016125.1:g.18725GT[12], NG_016125.1:g.18725GT[13], NG_016125.1:g.18725GT[14], NG_016125.1:g.18725GT[15], NG_016125.1:g.18725GT[16], NG_016125.1:g.18725GT[18], NG_016125.1:g.18725GT[19], NG_016125.1:g.18725GT[20], NG_016125.1:g.18725GT[21], NG_016125.1:g.18725GT[22], NG_016125.1:g.18725GT[23], NG_016125.1:g.18725GT[24], NG_016125.1:g.18725GT[25]

Select item 149107841711.

rs1491078417 has merged into rs34602155 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:119656388 (GRCh38)
10:121415900 (GRCh37)
Canonical SPDI:: NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.5/20 (GENOME_DK)
HGVS:: NC_000010.11:g.119656388_119656398del, NC_000010.11:g.119656389_119656398del, NC_000010.11:g.119656390_119656398del, NC_000010.11:g.119656391_119656398del, NC_000010.11:g.119656394_119656398del, NC_000010.11:g.119656395_119656398del, NC_000010.11:g.119656396_119656398del, NC_000010.11:g.119656397_119656398del, NC_000010.11:g.119656398del, NC_000010.11:g.119656398dup, NC_000010.11:g.119656397_119656398dup, NC_000010.11:g.119656396_119656398dup, NC_000010.11:g.119656395_119656398dup, NC_000010.11:g.119656394_119656398dup, NC_000010.11:g.119656393_119656398dup, NC_000010.10:g.121415900_121415910del, NC_000010.10:g.121415901_121415910del, NC_000010.10:g.121415902_121415910del, NC_000010.10:g.121415903_121415910del, NC_000010.10:g.121415906_121415910del, NC_000010.10:g.121415907_121415910del, NC_000010.10:g.121415908_121415910del, NC_000010.10:g.121415909_121415910del, NC_000010.10:g.121415910del, NC_000010.10:g.121415910dup, NC_000010.10:g.121415909_121415910dup, NC_000010.10:g.121415908_121415910dup, NC_000010.10:g.121415907_121415910dup, NC_000010.10:g.121415906_121415910dup, NC_000010.10:g.121415905_121415910dup, NG_016125.1:g.10019_10029del, NG_016125.1:g.10020_10029del, NG_016125.1:g.10021_10029del, NG_016125.1:g.10022_10029del, NG_016125.1:g.10025_10029del, NG_016125.1:g.10026_10029del, NG_016125.1:g.10027_10029del, NG_016125.1:g.10028_10029del, NG_016125.1:g.10029del, NG_016125.1:g.10029dup, NG_016125.1:g.10028_10029dup, NG_016125.1:g.10027_10029dup, NG_016125.1:g.10026_10029dup, NG_016125.1:g.10025_10029dup, NG_016125.1:g.10024_10029dup

Select item 149105284912.

rs1491052849 has merged into rs111712526 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTTT [Show Flanks]
Chromosome:: 10:119665092 (GRCh38)
10:121424604 (GRCh37)
Canonical SPDI:: NC_000010.11:119665090:TTT:T,NC_000010.11:119665090:TTT:TT,NC_000010.11:119665090:TTT:TTTT,NC_000010.11:119665090:TTT:TTTTTT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.119665092_119665093del, NC_000010.11:g.119665093del, NC_000010.11:g.119665093dup, NC_000010.11:g.119665091_119665093dup, NC_000010.10:g.121424604_121424605del, NC_000010.10:g.121424605del, NC_000010.10:g.121424605dup, NC_000010.10:g.121424603_121424605dup, NG_016125.1:g.18723_18724del, NG_016125.1:g.18724del, NG_016125.1:g.18724dup, NG_016125.1:g.18722_18724dup

Select item 149092115213.

rs1490921152 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:119663859 (GRCh38)
10:121423371 (GRCh37)
Canonical SPDI:: NC_000010.11:119663858:C:A,NC_000010.11:119663858:C:T
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.119663859C>A, NC_000010.11:g.119663859C>T, NC_000010.10:g.121423371C>A, NC_000010.10:g.121423371C>T, NG_016125.1:g.17490C>A, NG_016125.1:g.17490C>T

Select item 149084977514.

rs1490849775 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 10:119664807 (GRCh38)
10:121424319 (GRCh37)
Canonical SPDI:: NC_000010.11:119664806:TTTTTT:TTTTT
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.119664812del, NC_000010.10:g.121424324del, NG_016125.1:g.18443del

Select item 149074140415.

rs1490741404 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:119671311 (GRCh38)
10:121430823 (GRCh37)
Canonical SPDI:: NC_000010.11:119671310:T:C
Gene:: BAG3 (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.119671311T>C, NC_000010.10:g.121430823T>C, NG_016125.1:g.24942T>C

Select item 149066152716.

rs1490661527 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 10:119657879 (GRCh38)
10:121417391 (GRCh37)
Canonical SPDI:: NC_000010.11:119657878:G:
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000019/5 (TOPMED)
HGVS:: NC_000010.11:g.119657879del, NC_000010.10:g.121417391del, NG_016125.1:g.11510del

Select item 149063296717.

rs1490632967 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:119670240 (GRCh38)
10:121429752 (GRCh37)
Canonical SPDI:: NC_000010.11:119670239:C:T
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000010.11:g.119670240C>T, NC_000010.10:g.121429752C>T, NG_016125.1:g.23871C>T

Select item 149054554518.

rs1490545545 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 10:119662925 (GRCh38)
10:121422437 (GRCh37)
Canonical SPDI:: NC_000010.11:119662924:G:A,NC_000010.11:119662924:G:C,NC_000010.11:119662924:G:T
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.119662925G>A, NC_000010.11:g.119662925G>C, NC_000010.11:g.119662925G>T, NC_000010.10:g.121422437G>A, NC_000010.10:g.121422437G>C, NC_000010.10:g.121422437G>T, NG_016125.1:g.16556G>A, NG_016125.1:g.16556G>C, NG_016125.1:g.16556G>T

Select item 149039156519.

rs1490391565 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:119663411 (GRCh38)
10:121422923 (GRCh37)
Canonical SPDI:: NC_000010.11:119663410:T:C
Gene:: BAG3 (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.119663411T>C, NC_000010.10:g.121422923T>C, NG_016125.1:g.17042T>C

Select item 149031839820.

rs1490318398 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:119663793 (GRCh38)
10:121423305 (GRCh37)
Canonical SPDI:: NC_000010.11:119663792:G:A
Gene:: BAG3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.119663793G>A, NC_000010.10:g.121423305G>A, NG_016125.1:g.17424G>A

<< First< Prev

Page of 376

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 7502

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity