Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.17027750_17028737delCA645509076SDHBc.117_369+1del
c.246_498+1del
c.288_540+1del
n.205_458del
n.276_474+1del
 ClinVar
1g.17028722A>CCA338275123SDHBc.130T>G (p.Cys44Gly)
c.259T>G (p.Cys87Gly)
c.301T>G (p.Cys101Gly)
n.218T>G
n.289T>G
1g.17028722A>GCA338275122SDHBc.130T>C (p.Cys44Arg)
c.259T>C (p.Cys87Arg)
c.301T>C (p.Cys101Arg)
n.218T>C
n.289T>C
1g.17028722A>TCA338275120SDHBc.130T>A (p.Cys44Ser)
c.259T>A (p.Cys87Ser)
c.301T>A (p.Cys101Ser)
n.218T>A
n.289T>A
1g.17028723delCA2586966133SDHBc.130del (p.Cys44ValfsTer3)
c.259del (p.Cys87ValfsTer3)
c.301del (p.Cys101ValfsTer3)
n.218del
n.289del
1g.17028723A=CA1140263948SDHBc.129T= (p.Ser43=)
c.258T= (p.Ser86=)
c.300T= (p.Ser100=)
n.217T=
n.288T=
1g.17028723A>CCA416088103SDHBc.129T>G (p.Ser43=)
c.258T>G (p.Ser86=)
c.300T>G (p.Ser100=)
n.217T>G
n.288T>G
1g.17028723A>GCA015729SDHBc.129T>C (p.Ser43=)
c.258T>C (p.Ser86=)
c.300T>C (p.Ser100=)
n.217T>C
n.288T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.17028723A>TCA416088107SDHBc.129T>A (p.Ser43=)
c.258T>A (p.Ser86=)
c.300T>A (p.Ser100=)
n.217T>A
n.288T>A
1g.17028724G>ACA015720SDHBc.128C>T (p.Ser43Phe)
c.257C>T (p.Ser86Phe)
c.299C>T (p.Ser100Phe)
n.216C>T
n.287C>T
 ClinVar dbSNP
1g.17028724G>CCA338275124SDHBc.128C>G (p.Ser43Cys)
c.257C>G (p.Ser86Cys)
c.299C>G (p.Ser100Cys)
n.216C>G
n.287C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
1g.17028724G=CA1141580615SDHBc.128C= (p.Ser43=)
c.257C= (p.Ser86=)
c.299C= (p.Ser100=)
n.216C=
n.287C=
1g.17028724G>TCA338275131SDHBc.128C>A (p.Ser43Tyr)
c.257C>A (p.Ser86Tyr)
c.299C>A (p.Ser100Tyr)
n.216C>A
n.287C>A
1g.17028725A>CCA338275136SDHBc.127T>G (p.Ser43Ala)
c.256T>G (p.Ser86Ala)
c.298T>G (p.Ser100Ala)
n.215T>G
n.286T>G
1g.17028725A>GCA338275142SDHBc.127T>C (p.Ser43Pro)
c.256T>C (p.Ser86Pro)
c.298T>C (p.Ser100Pro)
n.215T>C
n.286T>C
 gnomAD v4
1g.17028725A>TCA338275144SDHBc.127T>A (p.Ser43Thr)
c.256T>A (p.Ser86Thr)
c.298T>A (p.Ser100Thr)
n.215T>A
n.286T>A
1g.17028726delCA658655530SDHBc.126del (p.Ser43LeufsTer4)
c.255del (p.Ser86LeufsTer4)
c.297del (p.Ser100LeufsTer4)
n.214del
n.285del
 gnomAD v4
1g.17028726G>ACA416088118SDHBc.126C>T (p.Gly42=)
c.255C>T (p.Gly85=)
c.297C>T (p.Gly99=)
n.214C>T
n.285C>T
1g.17028726G>CCA416088122SDHBc.126C>G (p.Gly42=)
c.255C>G (p.Gly85=)
c.297C>G (p.Gly99=)
n.214C>G
n.285C>G
 ClinVar
1g.17028726G>TCA416088120SDHBc.126C>A (p.Gly42=)
c.255C>A (p.Gly85=)
c.297C>A (p.Gly99=)
n.214C>A
n.285C>A
1g.17028727C>ACA338275155SDHBc.125G>T (p.Gly42Val)
c.254G>T (p.Gly85Val)
c.296G>T (p.Gly99Val)
n.213G>T
n.284G>T
 dbSNP
1g.17028727C=CA1156080536SDHBc.125G= (p.Gly42=)
c.254G= (p.Gly85=)
c.296G= (p.Gly99=)
n.213G=
n.284G=
1g.17028727C>GCA338275157SDHBc.125G>C (p.Gly42Ala)
c.254G>C (p.Gly85Ala)
c.296G>C (p.Gly99Ala)
n.213G>C
n.284G>C
1g.17028727C>TCA10581747SDHBc.125G>A (p.Gly42Asp)
c.254G>A (p.Gly85Asp)
c.296G>A (p.Gly99Asp)
n.213G>A
n.284G>A
 ClinVar dbSNP
1g.17028727_17028746delinsCCACAGATGCCTGAAAGAGACA1156080537SDHBc.116-10_125delinsTCTCTTTCAGGCATCTGTGG
c.245-10_254delinsTCTCTTTCAGGCATCTGTGG
c.287-10_296delinsTCTCTTTCAGGCATCTGTGG
n.204-10_213delinsTCTCTTTCAGGCATCTGTGG
n.275-10_284delinsTCTCTTTCAGGCATCTGTGG
1g.17028728C>ACA338275166SDHBc.124G>T (p.Gly42Cys)
c.253G>T (p.Gly85Cys)
c.295G>T (p.Gly99Cys)
n.212G>T
n.283G>T
1g.17028728C=CA1156080538SDHBc.124G= (p.Gly42=)
c.253G= (p.Gly85=)
c.295G= (p.Gly99=)
n.212G=
n.283G=
1g.17028728C>GCA338275177SDHBc.124G>C (p.Gly42Arg)
c.253G>C (p.Gly85Arg)
c.295G>C (p.Gly99Arg)
n.212G>C
n.283G>C
1g.17028728C>TCA18666849SDHBc.124G>A (p.Gly42Ser)
c.253G>A (p.Gly85Ser)
c.295G>A (p.Gly99Ser)
n.212G>A
n.283G>A
 ClinVar dbSNP
1g.17028732_17028750delCA1156080539SDHBc.116-10_124del
c.245-10_253del
c.287-10_295del
n.204-10_212del
n.275-10_283del
 ClinVar dbSNP
1g.17028729A>CCA338275187SDHBc.123T>G (p.Cys41Trp)
c.252T>G (p.Cys84Trp)
c.294T>G (p.Cys98Trp)
n.211T>G
n.282T>G
1g.17028729A>GCA416088133SDHBc.123T>C (p.Cys41=)
c.252T>C (p.Cys84=)
c.294T>C (p.Cys98=)
n.211T>C
n.282T>C
 COSMIC
1g.17028729A>TCA338275191SDHBc.123T>A (p.Cys41Ter)
c.252T>A (p.Cys84Ter)
c.294T>A (p.Cys98Ter)
n.211T>A
n.282T>A
1g.17028730C>ACA338275203SDHBc.122G>T (p.Cys41Phe)
c.251G>T (p.Cys84Phe)
c.293G>T (p.Cys98Phe)
n.210G>T
n.281G>T
1g.17028730C=CA1156080540SDHBc.122G= (p.Cys41=)
c.251G= (p.Cys84=)
c.293G= (p.Cys98=)
n.210G=
n.281G=
1g.17028730C>GCA338275194SDHBc.122G>C (p.Cys41Ser)
c.251G>C (p.Cys84Ser)
c.293G>C (p.Cys98Ser)
n.210G>C
n.281G>C
1g.17028730C>TCA338275198SDHBc.122G>A (p.Cys41Tyr)
c.251G>A (p.Cys84Tyr)
c.293G>A (p.Cys98Tyr)
n.210G>A
n.281G>A
 ClinVar dbSNP
1g.17028731A>CCA338275206SDHBc.121T>G (p.Cys41Gly)
c.250T>G (p.Cys84Gly)
c.292T>G (p.Cys98Gly)
n.209T>G
n.280T>G
1g.17028731A>GCA338275224SDHBc.121T>C (p.Cys41Arg)
c.250T>C (p.Cys84Arg)
c.292T>C (p.Cys98Arg)
n.209T>C
n.280T>C
 ClinVar
1g.17028731A>TCA338275228SDHBc.121T>A (p.Cys41Ser)
c.250T>A (p.Cys84Ser)
c.292T>A (p.Cys98Ser)
n.209T>A
n.280T>A
1g.17028732G>ACA416088138SDHBc.120C>T (p.Ile40=)
c.249C>T (p.Ile83=)
c.291C>T (p.Ile97=)
n.208C>T
n.279C>T
 ClinVar dbSNP gnomAD v4
1g.17028732G>CCA338275241SDHBc.120C>G (p.Ile40Met)
c.249C>G (p.Ile83Met)
c.291C>G (p.Ile97Met)
n.208C>G
n.279C>G
 dbSNP
1g.17028732G=CA1156080541SDHBc.120C= (p.Ile40=)
c.249C= (p.Ile83=)
c.291C= (p.Ile97=)
n.208C=
n.279C=
1g.17028732G>TCA416088135SDHBc.120C>A (p.Ile40=)
c.249C>A (p.Ile83=)
c.291C>A (p.Ile97=)
n.208C>A
n.279C>A
1g.17028733A>CCA338275246SDHBc.119T>G (p.Ile40Ser)
c.248T>G (p.Ile83Ser)
c.290T>G (p.Ile97Ser)
n.207T>G
n.278T>G
1g.17028733A>GCA338275249SDHBc.119T>C (p.Ile40Thr)
c.248T>C (p.Ile83Thr)
c.290T>C (p.Ile97Thr)
n.207T>C
n.278T>C
1g.17028733A>TCA338275263SDHBc.119T>A (p.Ile40Asn)
c.248T>A (p.Ile83Asn)
c.290T>A (p.Ile97Asn)
n.207T>A
n.278T>A
1g.17028734T>ACA338275267SDHBc.118A>T (p.Ile40Phe)
c.247A>T (p.Ile83Phe)
c.289A>T (p.Ile97Phe)
n.206A>T
n.277A>T
 ClinVar dbSNP
1g.17028734T>CCA338275269SDHBc.118A>G (p.Ile40Val)
c.247A>G (p.Ile83Val)
c.289A>G (p.Ile97Val)
n.206A>G
n.277A>G
 gnomAD v4
1g.17028734T>GCA338275270SDHBc.118A>C (p.Ile40Leu)
c.247A>C (p.Ile83Leu)
c.289A>C (p.Ile97Leu)
n.206A>C
n.277A>C

Number of alleles fetched