Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.46756451_46756620delinsAGGCTGCGGGCGTGCGCTACTGGCTCGAGGGCGGCTCACTGCTGGGGGCCGCCCGCCACGGGGACATCATCCCATGGGACTACGACGTGGACCTGGGCATCTACTTGGAGGACGTGGGCAACTGCGAGCAGCTGCGGGGGGCAGAGGCCGGCTCGGTGGTGGATGAGCGCCA2339067617FKRPc.1001_1170delinsAGGCTGCGGGCGTGCGCTACTGGCTCGAGGGCGGCTCACTGCTGGGGGCCGCCCGCCACGGGGACATCATCCCATGGGACTACGACGTGGACCTGGGCATCTACTTGGAGGACGTGGGCAACTGCGAGCAGCTGCGGGGGGCAGAGGCCGGCTCGGTGGTGGATGAGCGC (p.Glu334=)
n.247-5382_247-5213delinsAGGCTGCGGGCGTGCGCTACTGGCTCGAGGGCGGCTCACTGCTGGGGGCCGCCCGCCACGGGGACATCATCCCATGGGACTACGACGTGGACCTGGGCATCTACTTGGAGGACGTGGGCAACTGCGAGCAGCTGCGGGGGGCAGAGGCCGGCTCGGTGGTGGATGAGCGC
n.247+7786_247+7955delinsAGGCTGCGGGCGTGCGCTACTGGCTCGAGGGCGGCTCACTGCTGGGGGCCGCCCGCCACGGGGACATCATCCCATGGGACTACGACGTGGACCTGGGCATCTACTTGGAGGACGTGGGCAACTGCGAGCAGCTGCGGGGGGCAGAGGCCGGCTCGGTGGTGGATGAGCGC
19g.46756456_46756624delCA915951961FKRPc.1006_1174del (p.Ala336SerfsTer?)
n.247-5377_247-5209del
n.247+7791_247+7959del
ClinVar dbSNP
19g.46756525delCA2573156480FKRPc.1075del (p.Trp359GlyfsTer?)
n.247-5308del
n.247+7860del
ClinVar dbSNP
19g.46756525T>ACA406496593FKRPc.1075T>A (p.Trp359Arg)
n.247-5308T>A
n.247+7860T>A
19g.46756525T>CCA406496592FKRPc.1075T>C (p.Trp359Arg)
n.247-5308T>C
n.247+7860T>C
ClinVar dbSNP
19g.46756525T>GCA406496591FKRPc.1075T>G (p.Trp359Gly)
n.247-5308T>G
n.247+7860T>G
19g.46756525T=CA2339067671FKRPc.1075T= (p.Trp359=)
n.247-5308T=
n.247+7860T=
19g.46756526G>ACA406496594FKRPc.1076G>A (p.Trp359Ter)
n.247-5307G>A
n.247+7861G>A
19g.46756526G>CCA406496595FKRPc.1076G>C (p.Trp359Ser)
n.247-5307G>C
n.247+7861G>C
19g.46756526G>TCA406496596FKRPc.1076G>T (p.Trp359Leu)
n.247-5307G>T
n.247+7861G>T
19g.46756527_46756528dupCA891844245FKRPc.1077_1078dup (p.Asp360GlyfsTer?)
n.247-5306_247-5305dup
n.247+7862_247+7863dup
ClinVar dbSNP
19g.46756527G>ACA406496597FKRPc.1077G>A (p.Trp359Ter)
n.247-5306G>A
n.247+7862G>A
dbSNP
19g.46756527G>CCA406496598FKRPc.1077G>C (p.Trp359Cys)
n.247-5306G>C
n.247+7862G>C
19g.46756527G=CA2339067672FKRPc.1077G= (p.Trp359=)
n.247-5306G=
n.247+7862G=
19g.46756527G>TCA406496599FKRPc.1077G>T (p.Trp359Cys)
n.247-5306G>T
n.247+7862G>T
19g.46756528G>ACA406496600FKRPc.1078G>A (p.Asp360Asn)
n.247-5305G>A
n.247+7863G>A
dbSNP gnomAD v2 gnomAD v4
19g.46756528G>CCA9532239FKRPc.1078G>C (p.Asp360His)
n.247-5305G>C
n.247+7863G>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.46756528G=CA2339067673FKRPc.1078G= (p.Asp360=)
n.247-5305G=
n.247+7863G=
19g.46756528G>TCA406496601FKRPc.1078G>T (p.Asp360Tyr)
n.247-5305G>T
n.247+7863G>T
dbSNP
19g.46756529A=CA2339067674FKRPc.1079A= (p.Asp360=)
n.247-5304A=
n.247+7864A=
19g.46756529A>CCA406496602FKRPc.1079A>C (p.Asp360Ala)
n.247-5304A>C
n.247+7864A>C
19g.46756529A>GCA406496603FKRPc.1079A>G (p.Asp360Gly)
n.247-5304A>G
n.247+7864A>G
19g.46756529A>TCA9532240FKRPc.1079A>T (p.Asp360Val)
n.247-5304A>T
n.247+7864A>T
dbSNP ExAC gnomAD v2 gnomAD v4
19g.46756530C>ACA406496604FKRPc.1080C>A (p.Asp360Glu)
n.247-5303C>A
n.247+7865C>A
gnomAD v4
19g.46756530C>GCA406496605FKRPc.1080C>G (p.Asp360Glu)
n.247-5303C>G
n.247+7865C>G
19g.46756530C>TCA507975990FKRPc.1080C>T (p.Asp360=)
n.247-5303C>T
n.247+7865C>T
19g.46756531T>ACA406496606FKRPc.1081T>A (p.Tyr361Asn)
n.247-5302T>A
n.247+7866T>A
19g.46756531T>CCA406496607FKRPc.1081T>C (p.Tyr361His)
n.247-5302T>C
n.247+7866T>C
19g.46756531T>GCA406496608FKRPc.1081T>G (p.Tyr361Asp)
n.247-5302T>G
n.247+7866T>G
19g.46756532A=CA2339067675FKRPc.1082A= (p.Tyr361=)
n.247-5301A=
n.247+7867A=
19g.46756532A>CCA309099750FKRPc.1082A>C (p.Tyr361Ser)
n.247-5301A>C
n.247+7867A>C
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.46756532A>GCA406496609FKRPc.1082A>G (p.Tyr361Cys)
n.247-5301A>G
n.247+7867A>G
19g.46756532A>TCA406496610FKRPc.1082A>T (p.Tyr361Phe)
n.247-5301A>T
n.247+7867A>T
19g.46756533delCA2576826108FKRPc.1083del (p.Tyr361Ter)
n.247-5300del
n.247+7868del
19g.46756533C>ACA16616286FKRPc.1083C>A (p.Tyr361Ter)
n.247-5300C>A
n.247+7868C>A
ClinVar dbSNP
19g.46756533C=CA2339067676FKRPc.1083C= (p.Tyr361=)
n.247-5300C=
n.247+7868C=
19g.46756533C>GCA406496611FKRPc.1083C>G (p.Tyr361Ter)
n.247-5300C>G
n.247+7868C>G
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.46756533C>TCA507975995FKRPc.1083C>T (p.Tyr361=)
n.247-5300C>T
n.247+7868C>T
ClinVar dbSNP gnomAD v4
19g.46756534G>ACA406496612FKRPc.1084G>A (p.Asp362Asn)
n.247-5299G>A
n.247+7869G>A
dbSNP gnomAD v2 gnomAD v4
19g.46756534G>CCA406496614FKRPc.1084G>C (p.Asp362His)
n.247-5299G>C
n.247+7869G>C
dbSNP
19g.46756534G=CA2339067677FKRPc.1084G= (p.Asp362=)
n.247-5299G=
n.247+7869G=
19g.46756534G>TCA406496613FKRPc.1084G>T (p.Asp362Tyr)
n.247-5299G>T
n.247+7869G>T
19g.46756535A>CCA406496615FKRPc.1085A>C (p.Asp362Ala)
n.247-5298A>C
n.247+7870A>C
19g.46756535A>GCA406496616FKRPc.1085A>G (p.Asp362Gly)
n.247-5298A>G
n.247+7870A>G
19g.46756535A>TCA406496617FKRPc.1085A>T (p.Asp362Val)
n.247-5298A>T
n.247+7870A>T
gnomAD v4
19g.46756536C>ACA406496618FKRPc.1086C>A (p.Asp362Glu)
n.247-5297C>A
n.247+7871C>A
ClinVar dbSNP
19g.46756536C=CA2339067678FKRPc.1086C= (p.Asp362=)
n.247-5297C=
n.247+7871C=
19g.46756536C>GCA406496619FKRPc.1086C>G (p.Asp362Glu)
n.247-5297C>G
n.247+7871C>G
19g.46756536C>TCA9532241FKRPc.1086C>T (p.Asp362=)
n.247-5297C>T
n.247+7871C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.46756537G>ACA406496620FKRPc.1087G>A (p.Val363Met)
n.247-5296G>A
n.247+7872G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched