SNP Links for Gene (Select 6390) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915574431.

rs1491557443 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTA,TTTTTA,TTTTTTTAAA [Show Flanks]
Chromosome:: 1:17042979 (GRCh38)
1:17369475 (GRCh37)
Canonical SPDI:: NC_000001.11:17042979::TTA,NC_000001.11:17042979::TTTTTA,NC_000001.11:17042979::TTTTTTTAAA
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.17042979_17042980insTTA, NC_000001.11:g.17042979_17042980insTTTTTA, NC_000001.11:g.17042979_17042980insTTTTTTTAAA, NC_000001.10:g.17369474_17369475insTTA, NC_000001.10:g.17369474_17369475insTTTTTA, NC_000001.10:g.17369474_17369475insTTTTTTTAAA, NG_012340.1:g.16191_16192insTAA, NG_012340.1:g.16191_16192insTAAAAA, NG_012340.1:g.16191_16192insTTTAAAAAAA, NW_025791756.1:g.1458170_1458171insTTA, NW_025791756.1:g.1458170_1458171insTTTTTA, NW_025791756.1:g.1458170_1458171insTTTTTTTAAA

Select item 14913030962.

rs1491303096 [Homo sapiens]

Variant type:: INS
Alleles:: ->GATTAC [Show Flanks]
Chromosome:: 1:17050378 (GRCh38)
1:17376874 (GRCh37)
Canonical SPDI:: NC_000001.11:17050378::GATTAC
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GATTAC=0.001041/17 (ALFA)
GATTAC=0.003795/17 (Estonian)
GATTAC=0.005153/33 (1000Genomes)
GATTAC=0.010115/1416 (GnomAD)
GATTAC=0.02/12 (NorthernSweden)
HGVS:: NC_000001.11:g.17050378_17050379insGATTAC, NC_000001.10:g.17376873_17376874insGATTAC, NG_012340.1:g.8792_8793insGTAATC, NW_025791756.1:g.1465569_1465570insGATTAC

Select item 14912810763.

rs1491281076 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT [Show Flanks]
Chromosome:: 1:17049648 (GRCh38)
1:17376144 (GRCh37)
Canonical SPDI:: NC_000001.11:17049648:T:TAT
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.17049649_17049650insAT, NC_000001.10:g.17376144_17376145insAT, NG_012340.1:g.9522_9523insTA, NW_025791756.1:g.1464840_1464841insAT

Select item 14912610644.

rs1491261064 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:17042979 (GRCh38)
1:17369474 (GRCh37)
Canonical SPDI:: NC_000001.11:17042978:TG:
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.004721/56 (ALFA)
-=0.000237/29 (GnomAD)
-=0.000505/14 (TOMMO)
HGVS:: NC_000001.11:g.17042979_17042980del, NC_000001.10:g.17369474_17369475del, NG_012340.1:g.16191_16192del, NW_025791756.1:g.1458170_1458171del

Select item 14912384125.

rs1491238412 has merged into rs397835910 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:17049659 (GRCh38)
1:17376154 (GRCh37)
Canonical SPDI:: NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:17049647:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.17049659_17049677del, NC_000001.11:g.17049660_17049677del, NC_000001.11:g.17049661_17049677del, NC_000001.11:g.17049662_17049677del, NC_000001.11:g.17049663_17049677del, NC_000001.11:g.17049664_17049677del, NC_000001.11:g.17049665_17049677del, NC_000001.11:g.17049666_17049677del, NC_000001.11:g.17049667_17049677del, NC_000001.11:g.17049668_17049677del, NC_000001.11:g.17049669_17049677del, NC_000001.11:g.17049670_17049677del, NC_000001.11:g.17049671_17049677del, NC_000001.11:g.17049672_17049677del, NC_000001.11:g.17049673_17049677del, NC_000001.11:g.17049674_17049677del, NC_000001.11:g.17049675_17049677del, NC_000001.11:g.17049676_17049677del, NC_000001.11:g.17049677del, NC_000001.11:g.17049677dup, NC_000001.11:g.17049676_17049677dup, NC_000001.11:g.17049675_17049677dup, NC_000001.11:g.17049674_17049677dup, NC_000001.11:g.17049673_17049677dup, NC_000001.11:g.17049672_17049677dup, NC_000001.11:g.17049671_17049677dup, NC_000001.11:g.17049670_17049677dup, NC_000001.11:g.17049669_17049677dup, NC_000001.11:g.17049668_17049677dup, NC_000001.11:g.17049667_17049677dup, NC_000001.11:g.17049666_17049677dup, NC_000001.11:g.17049665_17049677dup, NC_000001.11:g.17049664_17049677dup, NC_000001.11:g.17049663_17049677dup, NC_000001.11:g.17049662_17049677dup, NC_000001.11:g.17049661_17049677dup, NC_000001.11:g.17049660_17049677dup, NC_000001.11:g.17049659_17049677dup, NC_000001.11:g.17049658_17049677dup, NC_000001.11:g.17049657_17049677dup, NC_000001.11:g.17049656_17049677dup, NC_000001.11:g.17049655_17049677dup, NC_000001.11:g.17049654_17049677dup, NC_000001.11:g.17049653_17049677dup, NC_000001.11:g.17049652_17049677dup, NC_000001.11:g.17049651_17049677dup, NC_000001.11:g.17049648_17049677dup, NC_000001.11:g.17049677_17049678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.17049677_17049678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.17049677_17049678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.17049677_17049678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.17049677_17049678insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.17376154_17376172del, NC_000001.10:g.17376155_17376172del, NC_000001.10:g.17376156_17376172del, NC_000001.10:g.17376157_17376172del, NC_000001.10:g.17376158_17376172del, NC_000001.10:g.17376159_17376172del, NC_000001.10:g.17376160_17376172del, NC_000001.10:g.17376161_17376172del, NC_000001.10:g.17376162_17376172del, NC_000001.10:g.17376163_17376172del, NC_000001.10:g.17376164_17376172del, NC_000001.10:g.17376165_17376172del, NC_000001.10:g.17376166_17376172del, NC_000001.10:g.17376167_17376172del, NC_000001.10:g.17376168_17376172del, NC_000001.10:g.17376169_17376172del, NC_000001.10:g.17376170_17376172del, NC_000001.10:g.17376171_17376172del, NC_000001.10:g.17376172del, NC_000001.10:g.17376172dup, NC_000001.10:g.17376171_17376172dup, NC_000001.10:g.17376170_17376172dup, NC_000001.10:g.17376169_17376172dup, NC_000001.10:g.17376168_17376172dup, NC_000001.10:g.17376167_17376172dup, NC_000001.10:g.17376166_17376172dup, NC_000001.10:g.17376165_17376172dup, NC_000001.10:g.17376164_17376172dup, NC_000001.10:g.17376163_17376172dup, NC_000001.10:g.17376162_17376172dup, NC_000001.10:g.17376161_17376172dup, NC_000001.10:g.17376160_17376172dup, NC_000001.10:g.17376159_17376172dup, NC_000001.10:g.17376158_17376172dup, NC_000001.10:g.17376157_17376172dup, NC_000001.10:g.17376156_17376172dup, NC_000001.10:g.17376155_17376172dup, NC_000001.10:g.17376154_17376172dup, NC_000001.10:g.17376153_17376172dup, NC_000001.10:g.17376152_17376172dup, NC_000001.10:g.17376151_17376172dup, NC_000001.10:g.17376150_17376172dup, NC_000001.10:g.17376149_17376172dup, NC_000001.10:g.17376148_17376172dup, NC_000001.10:g.17376147_17376172dup, NC_000001.10:g.17376146_17376172dup, NC_000001.10:g.17376143_17376172dup, NC_000001.10:g.17376172_17376173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.17376172_17376173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.17376172_17376173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.17376172_17376173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.17376172_17376173insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_012340.1:g.9505_9523del, NG_012340.1:g.9506_9523del, NG_012340.1:g.9507_9523del, NG_012340.1:g.9508_9523del, NG_012340.1:g.9509_9523del, NG_012340.1:g.9510_9523del, NG_012340.1:g.9511_9523del, NG_012340.1:g.9512_9523del, NG_012340.1:g.9513_9523del, NG_012340.1:g.9514_9523del, NG_012340.1:g.9515_9523del, NG_012340.1:g.9516_9523del, NG_012340.1:g.9517_9523del, NG_012340.1:g.9518_9523del, NG_012340.1:g.9519_9523del, NG_012340.1:g.9520_9523del, NG_012340.1:g.9521_9523del, NG_012340.1:g.9522_9523del, NG_012340.1:g.9523del, NG_012340.1:g.9523dup, NG_012340.1:g.9522_9523dup, NG_012340.1:g.9521_9523dup, NG_012340.1:g.9520_9523dup, NG_012340.1:g.9519_9523dup, NG_012340.1:g.9518_9523dup, NG_012340.1:g.9517_9523dup, NG_012340.1:g.9516_9523dup, NG_012340.1:g.9515_9523dup, NG_012340.1:g.9514_9523dup, NG_012340.1:g.9513_9523dup, NG_012340.1:g.9512_9523dup, NG_012340.1:g.9511_9523dup, NG_012340.1:g.9510_9523dup, NG_012340.1:g.9509_9523dup, NG_012340.1:g.9508_9523dup, NG_012340.1:g.9507_9523dup, NG_012340.1:g.9506_9523dup, NG_012340.1:g.9505_9523dup, NG_012340.1:g.9504_9523dup, NG_012340.1:g.9503_9523dup, NG_012340.1:g.9502_9523dup, NG_012340.1:g.9501_9523dup, NG_012340.1:g.9500_9523dup, NG_012340.1:g.9499_9523dup, NG_012340.1:g.9498_9523dup, NG_012340.1:g.9497_9523dup, NG_012340.1:g.9494_9523dup, NG_012340.1:g.9523_9524insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012340.1:g.9523_9524insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012340.1:g.9523_9524insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012340.1:g.9523_9524insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012340.1:g.9523_9524insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_025791756.1:g.1464868dup, NW_025791756.1:g.1464851_1464868del, NW_025791756.1:g.1464852_1464868del, NW_025791756.1:g.1464853_1464868del, NW_025791756.1:g.1464854_1464868del, NW_025791756.1:g.1464855_1464868del, NW_025791756.1:g.1464856_1464868del, NW_025791756.1:g.1464857_1464868del, NW_025791756.1:g.1464858_1464868del, NW_025791756.1:g.1464859_1464868del, NW_025791756.1:g.1464860_1464868del, NW_025791756.1:g.1464861_1464868del, NW_025791756.1:g.1464862_1464868del, NW_025791756.1:g.1464863_1464868del, NW_025791756.1:g.1464864_1464868del, NW_025791756.1:g.1464865_1464868del, NW_025791756.1:g.1464866_1464868del, NW_025791756.1:g.1464867_1464868del, NW_025791756.1:g.1464868del, NW_025791756.1:g.1464867_1464868dup, NW_025791756.1:g.1464866_1464868dup, NW_025791756.1:g.1464865_1464868dup, NW_025791756.1:g.1464864_1464868dup, NW_025791756.1:g.1464863_1464868dup, NW_025791756.1:g.1464862_1464868dup, NW_025791756.1:g.1464861_1464868dup, NW_025791756.1:g.1464860_1464868dup, NW_025791756.1:g.1464859_1464868dup, NW_025791756.1:g.1464858_1464868dup, NW_025791756.1:g.1464857_1464868dup, NW_025791756.1:g.1464856_1464868dup, NW_025791756.1:g.1464855_1464868dup, NW_025791756.1:g.1464854_1464868dup, NW_025791756.1:g.1464853_1464868dup, NW_025791756.1:g.1464852_1464868dup, NW_025791756.1:g.1464851_1464868dup, NW_025791756.1:g.1464850_1464868dup, NW_025791756.1:g.1464849_1464868dup, NW_025791756.1:g.1464848_1464868dup, NW_025791756.1:g.1464847_1464868dup, NW_025791756.1:g.1464846_1464868dup, NW_025791756.1:g.1464845_1464868dup, NW_025791756.1:g.1464844_1464868dup, NW_025791756.1:g.1464843_1464868dup, NW_025791756.1:g.1464842_1464868dup, NW_025791756.1:g.1464841_1464868dup, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_025791756.1:g.1464868_1464869insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14911301336.

rs1491130133 has merged into rs1408023385 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAG>-,AG,AGAGAG [Show Flanks]
Chromosome:: 1:17047703 (GRCh38)
1:17374198 (GRCh37)
Canonical SPDI:: NC_000001.11:17047696:AGAGAGAGAG:AGAGAG,NC_000001.11:17047696:AGAGAGAGAG:AGAGAGAG,NC_000001.11:17047696:AGAGAGAGAG:AGAGAGAGAGAG
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAG=0./0 (ALFA)
AG=0.000035/1 (TOMMO)
-=0.000178/47 (TOPMED)
HGVS:: NC_000001.11:g.17047697AG[3], NC_000001.11:g.17047697AG[4], NC_000001.11:g.17047697AG[6], NC_000001.10:g.17374192AG[3], NC_000001.10:g.17374192AG[4], NC_000001.10:g.17374192AG[6], NG_012340.1:g.11465CT[3], NG_012340.1:g.11465CT[4], NG_012340.1:g.11465CT[6], NW_025791756.1:g.1462889AG[3], NW_025791756.1:g.1462889AG[4], NW_025791756.1:g.1462889AG[6]

Select item 14909950197.

rs1490995019 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:17047511 (GRCh38)
1:17374006 (GRCh37)
Canonical SPDI:: NC_000001.11:17047510:T:G
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.17047511T>G, NC_000001.10:g.17374006T>G, NG_012340.1:g.11660A>C, NW_025791756.1:g.1462702T>G

Select item 14908154398.

rs1490815439 has merged into rs1401779262 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 1:17030189 (GRCh38)
1:17356684 (GRCh37)
Canonical SPDI:: NC_000001.11:17030188:AAAAAAAA:AAAAAAA,NC_000001.11:17030188:AAAAAAAA:AAAAAAAAA
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.00011/2 (TOMMO)
-=0.00109/2 (Korea1K)
HGVS:: NC_000001.11:g.17030196del, NC_000001.11:g.17030196dup, NC_000001.10:g.17356691del, NC_000001.10:g.17356691dup, NG_012340.1:g.28982del, NG_012340.1:g.28982dup, NW_025791756.1:g.1445390del, NW_025791756.1:g.1445390dup

Select item 14908135319.

rs1490813531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:17039010 (GRCh38)
1:17365505 (GRCh37)
Canonical SPDI:: NC_000001.11:17039009:C:T
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.17039010C>T, NC_000001.10:g.17365505C>T, NG_012340.1:g.20161G>A, NW_025791756.1:g.1454202C>T

Select item 149078883310.

rs1490788833 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:17039933 (GRCh38)
1:17366428 (GRCh37)
Canonical SPDI:: NC_000001.11:17039932:C:G
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.17039933C>G, NC_000001.10:g.17366428C>G, NG_012340.1:g.19238G>C, NW_025791756.1:g.1455126C>G

Select item 149072465311.

rs1490724653 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGGC>- [Show Flanks]
Chromosome:: 1:17023215 (GRCh38)
1:17349710 (GRCh37)
Canonical SPDI:: NC_000001.11:17023212:GCAGGC:GC
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GC=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000015/4 (TOPMED)
-=0.000177/3 (TOMMO)
-=0.001092/2 (Korea1K)
HGVS:: NC_000001.11:g.17023215_17023218del, NC_000001.10:g.17349710_17349713del, NG_012340.1:g.35955_35958del, NW_025791756.1:g.1438409_1438412del

Select item 149065334612.

rs1490653346 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 1:17029126 (GRCh38)
1:17355621 (GRCh37)
Canonical SPDI:: NC_000001.11:17029125:G:
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000001.11:g.17029126del, NC_000001.10:g.17355621del, NG_012340.1:g.30045del, NW_025791756.1:g.1444320del

Select item 149061750213.

rs1490617502 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 1:17054694 (GRCh38)
1:17381189 (GRCh37)
Canonical SPDI:: NC_000001.11:17054693:C:
Gene:: SDHB (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.17054694del, NC_000001.10:g.17381189del, NG_012340.1:g.4477del, NW_025791756.1:g.1469890del

Select item 149060027114.

rs1490600271 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:17031225 (GRCh38)
1:17357720 (GRCh37)
Canonical SPDI:: NC_000001.11:17031224:A:T
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.17031225A>T, NC_000001.10:g.17357720A>T, NG_012340.1:g.27946T>A, NW_025791756.1:g.1446419A>T

Select item 149050358315.

rs1490503583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:17047901 (GRCh38)
1:17374396 (GRCh37)
Canonical SPDI:: NC_000001.11:17047900:G:A,NC_000001.11:17047900:G:C
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.17047901G>A, NC_000001.11:g.17047901G>C, NC_000001.10:g.17374396G>A, NC_000001.10:g.17374396G>C, NG_012340.1:g.11270C>T, NG_012340.1:g.11270C>G, NW_025791756.1:g.1463093G>A, NW_025791756.1:g.1463093G>C

Select item 149042137216.

rs1490421372 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:17045513 (GRCh38)
1:17372008 (GRCh37)
Canonical SPDI:: NC_000001.11:17045512:T:C
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.17045513T>C, NC_000001.10:g.17372008T>C, NG_012340.1:g.13658A>G, NW_025791756.1:g.1460704T>C

Select item 149034370317.

rs1490343703 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:17024510 (GRCh38)
1:17351005 (GRCh37)
Canonical SPDI:: NC_000001.11:17024509:A:G
Gene:: SDHB (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_000001.11:g.17024510A>G, NC_000001.10:g.17351005A>G, NG_012340.1:g.34661T>C, NW_025791756.1:g.1439704A>G

Select item 149032344818.

rs1490323448 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:17030989 (GRCh38)
1:17357484 (GRCh37)
Canonical SPDI:: NC_000001.11:17030988:A:G
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000091/12 (GnomAD)
HGVS:: NC_000001.11:g.17030989A>G, NC_000001.10:g.17357484A>G, NG_012340.1:g.28182T>C, NW_025791756.1:g.1446183A>G

Select item 149032038819.

rs1490320388 has merged into rs34561776 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:17039427 (GRCh38)
1:17365922 (GRCh37)
Canonical SPDI:: NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:17039415:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.17039427_17039437del, NC_000001.11:g.17039429_17039437del, NC_000001.11:g.17039431_17039437del, NC_000001.11:g.17039432_17039437del, NC_000001.11:g.17039435_17039437del, NC_000001.11:g.17039436_17039437del, NC_000001.11:g.17039437del, NC_000001.11:g.17039437dup, NC_000001.11:g.17039436_17039437dup, NC_000001.11:g.17039435_17039437dup, NC_000001.11:g.17039434_17039437dup, NC_000001.11:g.17039433_17039437dup, NC_000001.11:g.17039432_17039437dup, NC_000001.10:g.17365922_17365932del, NC_000001.10:g.17365924_17365932del, NC_000001.10:g.17365926_17365932del, NC_000001.10:g.17365927_17365932del, NC_000001.10:g.17365930_17365932del, NC_000001.10:g.17365931_17365932del, NC_000001.10:g.17365932del, NC_000001.10:g.17365932dup, NC_000001.10:g.17365931_17365932dup, NC_000001.10:g.17365930_17365932dup, NC_000001.10:g.17365929_17365932dup, NC_000001.10:g.17365928_17365932dup, NC_000001.10:g.17365927_17365932dup, NG_012340.1:g.19745_19755del, NG_012340.1:g.19747_19755del, NG_012340.1:g.19749_19755del, NG_012340.1:g.19750_19755del, NG_012340.1:g.19753_19755del, NG_012340.1:g.19754_19755del, NG_012340.1:g.19755del, NG_012340.1:g.19755dup, NG_012340.1:g.19754_19755dup, NG_012340.1:g.19753_19755dup, NG_012340.1:g.19752_19755dup, NG_012340.1:g.19751_19755dup, NG_012340.1:g.19750_19755dup, NW_025791756.1:g.1454620_1454630del, NW_025791756.1:g.1454622_1454630del, NW_025791756.1:g.1454624_1454630del, NW_025791756.1:g.1454625_1454630del, NW_025791756.1:g.1454628_1454630del, NW_025791756.1:g.1454629_1454630del, NW_025791756.1:g.1454630del, NW_025791756.1:g.1454630dup, NW_025791756.1:g.1454629_1454630dup, NW_025791756.1:g.1454628_1454630dup, NW_025791756.1:g.1454627_1454630dup, NW_025791756.1:g.1454626_1454630dup, NW_025791756.1:g.1454625_1454630dup

Select item 149029502720.

rs1490295027 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:17040613 (GRCh38)
1:17367108 (GRCh37)
Canonical SPDI:: NC_000001.11:17040612:C:T
Gene:: SDHB (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.17040613C>T, NC_000001.10:g.17367108C>T, NG_012340.1:g.18558G>A, NW_025791756.1:g.1455806C>T

<< First< Prev

Page of 50

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1000

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity