Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.38584992G>ACA024237RYR1c.1632G>A
c.3029G>A
c.3001G>A
n.89G>A
c.14696G>A (p.Gly4899Glu)
c.14681G>A (p.Gly4894Glu)
c.14678G>A (p.Gly4893Glu)
c.14663G>A (p.Gly4888Glu)
c.14693G>A (p.Gly4898Glu)
c.14609G>A (p.Gly4870Glu)
ClinVar dbSNP
19g.38584992G>CCA405690312RYR1c.1632G>C
c.3029G>C
c.3001G>C
n.89G>C
c.14696G>C (p.Gly4899Ala)
c.14681G>C (p.Gly4894Ala)
c.14678G>C (p.Gly4893Ala)
c.14663G>C (p.Gly4888Ala)
c.14693G>C (p.Gly4898Ala)
c.14609G>C (p.Gly4870Ala)
19g.38584992G=CA2335094951RYR1c.1632G=
c.3029G=
c.3001G=
n.89G=
c.14696G= (p.Gly4899=)
c.14681G= (p.Gly4894=)
c.14678G= (p.Gly4893=)
c.14663G= (p.Gly4888=)
c.14693G= (p.Gly4898=)
c.14609G= (p.Gly4870=)
19g.38584992G>TCA405690314RYR1c.1632G>T
c.3029G>T
c.3001G>T
n.89G>T
c.14696G>T (p.Gly4899Val)
c.14681G>T (p.Gly4894Val)
c.14678G>T (p.Gly4893Val)
c.14663G>T (p.Gly4888Val)
c.14693G>T (p.Gly4898Val)
c.14609G>T (p.Gly4870Val)
19g.38584993G>ACA061519RYR1c.1633G>A
c.3030G>A
c.3002G>A
n.90G>A
c.14697G>A (p.Gly4899=)
c.14682G>A (p.Gly4894=)
c.14679G>A (p.Gly4893=)
c.14664G>A (p.Gly4888=)
c.14694G>A (p.Gly4898=)
c.14610G>A (p.Gly4870=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.38584993G>CCA507246351RYR1c.1633G>C
c.3030G>C
c.3002G>C
n.90G>C
c.14697G>C (p.Gly4899=)
c.14682G>C (p.Gly4894=)
c.14679G>C (p.Gly4893=)
c.14664G>C (p.Gly4888=)
c.14694G>C (p.Gly4898=)
c.14610G>C (p.Gly4870=)
19g.38584993G=CA2335094952RYR1c.1633G=
c.3030G=
c.3002G=
n.90G=
c.14697G= (p.Gly4899=)
c.14682G= (p.Gly4894=)
c.14679G= (p.Gly4893=)
c.14664G= (p.Gly4888=)
c.14694G= (p.Gly4898=)
c.14610G= (p.Gly4870=)
19g.38584993G>TCA061521RYR1c.1633G>T
c.3030G>T
c.3002G>T
n.90G>T
c.14697G>T (p.Gly4899=)
c.14682G>T (p.Gly4894=)
c.14679G>T (p.Gly4893=)
c.14664G>T (p.Gly4888=)
c.14694G>T (p.Gly4898=)
c.14610G>T (p.Gly4870=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.38584994G>ACA405690320RYR1c.1634G>A
c.3031G>A
c.3003G>A
n.91G>A
c.14698G>A (p.Asp4900Asn)
c.14683G>A (p.Asp4895Asn)
c.14680G>A (p.Asp4894Asn)
c.14665G>A (p.Asp4889Asn)
c.14695G>A (p.Asp4899Asn)
c.14611G>A (p.Asp4871Asn)
19g.38584994G>CCA405690323RYR1c.1634G>C
c.3031G>C
c.3003G>C
n.91G>C
c.14698G>C (p.Asp4900His)
c.14683G>C (p.Asp4895His)
c.14680G>C (p.Asp4894His)
c.14665G>C (p.Asp4889His)
c.14695G>C (p.Asp4899His)
c.14611G>C (p.Asp4871His)
19g.38584994G>TCA405690327RYR1c.1634G>T
c.3031G>T
c.3003G>T
n.91G>T
c.14698G>T (p.Asp4900Tyr)
c.14683G>T (p.Asp4895Tyr)
c.14680G>T (p.Asp4894Tyr)
c.14665G>T (p.Asp4889Tyr)
c.14695G>T (p.Asp4899Tyr)
c.14611G>T (p.Asp4871Tyr)
19g.38584995A>CCA405690330RYR1c.1635A>C
c.3032A>C
c.3004A>C
n.92A>C
c.14699A>C (p.Asp4900Ala)
c.14684A>C (p.Asp4895Ala)
c.14681A>C (p.Asp4894Ala)
c.14666A>C (p.Asp4889Ala)
c.14696A>C (p.Asp4899Ala)
c.14612A>C (p.Asp4871Ala)
19g.38584995A>GCA405690333RYR1c.1635A>G
c.3032A>G
c.3004A>G
n.92A>G
c.14699A>G (p.Asp4900Gly)
c.14684A>G (p.Asp4895Gly)
c.14681A>G (p.Asp4894Gly)
c.14666A>G (p.Asp4889Gly)
c.14696A>G (p.Asp4899Gly)
c.14612A>G (p.Asp4871Gly)
dbSNP COSMIC
19g.38584995A>TCA405690342RYR1c.1635A>T
c.3032A>T
c.3004A>T
n.92A>T
c.14699A>T (p.Asp4900Val)
c.14684A>T (p.Asp4895Val)
c.14681A>T (p.Asp4894Val)
c.14666A>T (p.Asp4889Val)
c.14696A>T (p.Asp4899Val)
c.14612A>T (p.Asp4871Val)
19g.38584996C>ACA405690351RYR1c.1636C>A
c.3033C>A
c.3005C>A
n.93C>A
c.14700C>A (p.Asp4900Glu)
c.14685C>A (p.Asp4895Glu)
c.14682C>A (p.Asp4894Glu)
c.14667C>A (p.Asp4889Glu)
c.14697C>A (p.Asp4899Glu)
c.14613C>A (p.Asp4871Glu)
19g.38584996C=CA2335094953RYR1c.1636C=
c.3033C=
c.3005C=
n.93C=
c.14700C= (p.Asp4900=)
c.14685C= (p.Asp4895=)
c.14682C= (p.Asp4894=)
c.14667C= (p.Asp4889=)
c.14697C= (p.Asp4899=)
c.14613C= (p.Asp4871=)
19g.38584996C>GCA405690348RYR1c.1636C>G
c.3033C>G
c.3005C>G
n.93C>G
c.14700C>G (p.Asp4900Glu)
c.14685C>G (p.Asp4895Glu)
c.14682C>G (p.Asp4894Glu)
c.14667C>G (p.Asp4889Glu)
c.14697C>G (p.Asp4899Glu)
c.14613C>G (p.Asp4871Glu)
19g.38584996C>TCA081298RYR1c.1636C>T
c.3033C>T
c.3005C>T
n.93C>T
c.14700C>T (p.Asp4900=)
c.14685C>T (p.Asp4895=)
c.14682C>T (p.Asp4894=)
c.14667C>T (p.Asp4889=)
c.14697C>T (p.Asp4899=)
c.14613C>T (p.Asp4871=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.38584998_38585012dupCA2580097258RYR1c.1638_1652dup
c.3035_3049dup
c.3007_3021dup
n.95_109dup
c.14702_14716dup (p.Pro4905_Ala4906insGluIleGluAspPro)
c.14687_14701dup (p.Pro4900_Ala4901insGluIleGluAspPro)
c.14684_14698dup (p.Pro4899_Ala4900insGluIleGluAspPro)
c.14669_14683dup (p.Pro4894_Ala4895insGluIleGluAspPro)
c.14699_14713dup (p.Pro4904_Ala4905insGluIleGluAspPro)
c.14615_14629dup (p.Pro4876_Ala4877insGluIleGluAspPro)
ClinVar
19g.38584997G>ACA061530RYR1c.1637G>A
c.3034G>A
c.3006G>A
n.94G>A
c.14701G>A (p.Glu4901Lys)
c.14686G>A (p.Glu4896Lys)
c.14683G>A (p.Glu4895Lys)
c.14668G>A (p.Glu4890Lys)
c.14698G>A (p.Glu4900Lys)
c.14614G>A (p.Glu4872Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.38584997G>CCA405690362RYR1c.1637G>C
c.3034G>C
c.3006G>C
n.94G>C
c.14701G>C (p.Glu4901Gln)
c.14686G>C (p.Glu4896Gln)
c.14683G>C (p.Glu4895Gln)
c.14668G>C (p.Glu4890Gln)
c.14698G>C (p.Glu4900Gln)
c.14614G>C (p.Glu4872Gln)
19g.38584997G=CA2335094954RYR1c.1637G=
c.3034G=
c.3006G=
n.94G=
c.14701G= (p.Glu4901=)
c.14686G= (p.Glu4896=)
c.14683G= (p.Glu4895=)
c.14668G= (p.Glu4890=)
c.14698G= (p.Glu4900=)
c.14614G= (p.Glu4872=)
19g.38584997G>TCA405690358RYR1c.1637G>T
c.3034G>T
c.3006G>T
n.94G>T
c.14701G>T (p.Glu4901Ter)
c.14686G>T (p.Glu4896Ter)
c.14683G>T (p.Glu4895Ter)
c.14668G>T (p.Glu4890Ter)
c.14698G>T (p.Glu4900Ter)
c.14614G>T (p.Glu4872Ter)
19g.38584998A>CCA405690368RYR1c.1638A>C
c.3035A>C
c.3007A>C
n.95A>C
c.14702A>C (p.Glu4901Ala)
c.14687A>C (p.Glu4896Ala)
c.14684A>C (p.Glu4895Ala)
c.14669A>C (p.Glu4890Ala)
c.14699A>C (p.Glu4900Ala)
c.14615A>C (p.Glu4872Ala)
19g.38584998A>GCA405690371RYR1c.1638A>G
c.3035A>G
c.3007A>G
n.95A>G
c.14702A>G (p.Glu4901Gly)
c.14687A>G (p.Glu4896Gly)
c.14684A>G (p.Glu4895Gly)
c.14669A>G (p.Glu4890Gly)
c.14699A>G (p.Glu4900Gly)
c.14615A>G (p.Glu4872Gly)
19g.38584998A>TCA405690372RYR1c.1638A>T
c.3035A>T
c.3007A>T
n.95A>T
c.14702A>T (p.Glu4901Val)
c.14687A>T (p.Glu4896Val)
c.14684A>T (p.Glu4895Val)
c.14669A>T (p.Glu4890Val)
c.14699A>T (p.Glu4900Val)
c.14615A>T (p.Glu4872Val)
19g.38584999G>ACA507246355RYR1c.1639G>A
c.3036G>A
c.3008G>A
n.96G>A
c.14703G>A (p.Glu4901=)
c.14688G>A (p.Glu4896=)
c.14685G>A (p.Glu4895=)
c.14670G>A (p.Glu4890=)
c.14700G>A (p.Glu4900=)
c.14616G>A (p.Glu4872=)
19g.38584999G>CCA405690377RYR1c.1639G>C
c.3036G>C
c.3008G>C
n.96G>C
c.14703G>C (p.Glu4901Asp)
c.14688G>C (p.Glu4896Asp)
c.14685G>C (p.Glu4895Asp)
c.14670G>C (p.Glu4890Asp)
c.14700G>C (p.Glu4900Asp)
c.14616G>C (p.Glu4872Asp)
19g.38584999G>TCA405690380RYR1c.1639G>T
c.3036G>T
c.3008G>T
n.96G>T
c.14703G>T (p.Glu4901Asp)
c.14688G>T (p.Glu4896Asp)
c.14685G>T (p.Glu4895Asp)
c.14670G>T (p.Glu4890Asp)
c.14700G>T (p.Glu4900Asp)
c.14616G>T (p.Glu4872Asp)
19g.38585000A>CCA405690383RYR1c.1640A>C
c.3037A>C
c.3009A>C
n.97A>C
c.14704A>C (p.Ile4902Leu)
c.14689A>C (p.Ile4897Leu)
c.14686A>C (p.Ile4896Leu)
c.14671A>C (p.Ile4891Leu)
c.14701A>C (p.Ile4901Leu)
c.14617A>C (p.Ile4873Leu)
19g.38585000A>GCA405690384RYR1c.1640A>G
c.3037A>G
c.3009A>G
n.97A>G
c.14704A>G (p.Ile4902Val)
c.14689A>G (p.Ile4897Val)
c.14686A>G (p.Ile4896Val)
c.14671A>G (p.Ile4891Val)
c.14701A>G (p.Ile4901Val)
c.14617A>G (p.Ile4873Val)
19g.38585000A>TCA405690385RYR1c.1640A>T
c.3037A>T
c.3009A>T
n.97A>T
c.14704A>T (p.Ile4902Phe)
c.14689A>T (p.Ile4897Phe)
c.14686A>T (p.Ile4896Phe)
c.14671A>T (p.Ile4891Phe)
c.14701A>T (p.Ile4901Phe)
c.14617A>T (p.Ile4873Phe)
19g.38585001T>ACA405690386RYR1c.1641T>A
c.3038T>A
c.3010T>A
n.98T>A
c.14705T>A (p.Ile4902Asn)
c.14690T>A (p.Ile4897Asn)
c.14687T>A (p.Ile4896Asn)
c.14672T>A (p.Ile4891Asn)
c.14702T>A (p.Ile4901Asn)
c.14618T>A (p.Ile4873Asn)
19g.38585001T>CCA405690387RYR1c.1641T>C
c.3038T>C
c.3010T>C
n.98T>C
c.14705T>C (p.Ile4902Thr)
c.14690T>C (p.Ile4897Thr)
c.14687T>C (p.Ile4896Thr)
c.14672T>C (p.Ile4891Thr)
c.14702T>C (p.Ile4901Thr)
c.14618T>C (p.Ile4873Thr)
ClinVar dbSNP
19g.38585001T>GCA405690389RYR1c.1641T>G
c.3038T>G
c.3010T>G
n.98T>G
c.14705T>G (p.Ile4902Ser)
c.14690T>G (p.Ile4897Ser)
c.14687T>G (p.Ile4896Ser)
c.14672T>G (p.Ile4891Ser)
c.14702T>G (p.Ile4901Ser)
c.14618T>G (p.Ile4873Ser)
19g.38585001T=CA2335094955RYR1c.1641T=
c.3038T=
c.3010T=
n.98T=
c.14705T= (p.Ile4902=)
c.14690T= (p.Ile4897=)
c.14687T= (p.Ile4896=)
c.14672T= (p.Ile4891=)
c.14702T= (p.Ile4901=)
c.14618T= (p.Ile4873=)
19g.38585002C>ACA507246358RYR1c.1642C>A
c.3039C>A
c.3011C>A
n.99C>A
c.14706C>A (p.Ile4902=)
c.14691C>A (p.Ile4897=)
c.14688C>A (p.Ile4896=)
c.14673C>A (p.Ile4891=)
c.14703C>A (p.Ile4901=)
c.14619C>A (p.Ile4873=)
19g.38585002C=CA2335094956RYR1c.1642C=
c.3039C=
c.3011C=
n.99C=
c.14706C= (p.Ile4902=)
c.14691C= (p.Ile4897=)
c.14688C= (p.Ile4896=)
c.14673C= (p.Ile4891=)
c.14703C= (p.Ile4901=)
c.14619C= (p.Ile4873=)
19g.38585002C>GCA405690396RYR1c.1642C>G
c.3039C>G
c.3011C>G
n.99C>G
c.14706C>G (p.Ile4902Met)
c.14691C>G (p.Ile4897Met)
c.14688C>G (p.Ile4896Met)
c.14673C>G (p.Ile4891Met)
c.14703C>G (p.Ile4901Met)
c.14619C>G (p.Ile4873Met)
19g.38585002C>TCA10642775RYR1c.1642C>T
c.3039C>T
c.3011C>T
n.99C>T
c.14706C>T (p.Ile4902=)
c.14691C>T (p.Ile4897=)
c.14688C>T (p.Ile4896=)
c.14673C>T (p.Ile4891=)
c.14703C>T (p.Ile4901=)
c.14619C>T (p.Ile4873=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.38585003G>ACA061534RYR1c.1643G>A
c.3040G>A
c.3012G>A
n.100G>A
c.14707G>A (p.Glu4903Lys)
c.14692G>A (p.Glu4898Lys)
c.14689G>A (p.Glu4897Lys)
c.14674G>A (p.Glu4892Lys)
c.14704G>A (p.Glu4902Lys)
c.14620G>A (p.Glu4874Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.38585003G>CCA405690409RYR1c.1643G>C
c.3040G>C
c.3012G>C
n.100G>C
c.14707G>C (p.Glu4903Gln)
c.14692G>C (p.Glu4898Gln)
c.14689G>C (p.Glu4897Gln)
c.14674G>C (p.Glu4892Gln)
c.14704G>C (p.Glu4902Gln)
c.14620G>C (p.Glu4874Gln)
19g.38585003G=CA2335094957RYR1c.1643G=
c.3040G=
c.3012G=
n.100G=
c.14707G= (p.Glu4903=)
c.14692G= (p.Glu4898=)
c.14689G= (p.Glu4897=)
c.14674G= (p.Glu4892=)
c.14704G= (p.Glu4902=)
c.14620G= (p.Glu4874=)
19g.38585003G>TCA405690406RYR1c.1643G>T
c.3040G>T
c.3012G>T
n.100G>T
c.14707G>T (p.Glu4903Ter)
c.14692G>T (p.Glu4898Ter)
c.14689G>T (p.Glu4897Ter)
c.14674G>T (p.Glu4892Ter)
c.14704G>T (p.Glu4902Ter)
c.14620G>T (p.Glu4874Ter)
19g.38585004A>CCA405690410RYR1c.1644A>C
c.3041A>C
c.3013A>C
n.101A>C
c.14708A>C (p.Glu4903Ala)
c.14693A>C (p.Glu4898Ala)
c.14690A>C (p.Glu4897Ala)
c.14675A>C (p.Glu4892Ala)
c.14705A>C (p.Glu4902Ala)
c.14621A>C (p.Glu4874Ala)
19g.38585004A>GCA405690412RYR1c.1644A>G
c.3041A>G
c.3013A>G
n.101A>G
c.14708A>G (p.Glu4903Gly)
c.14693A>G (p.Glu4898Gly)
c.14690A>G (p.Glu4897Gly)
c.14675A>G (p.Glu4892Gly)
c.14705A>G (p.Glu4902Gly)
c.14621A>G (p.Glu4874Gly)
19g.38585004A>TCA405690414RYR1c.1644A>T
c.3041A>T
c.3013A>T
n.101A>T
c.14708A>T (p.Glu4903Val)
c.14693A>T (p.Glu4898Val)
c.14690A>T (p.Glu4897Val)
c.14675A>T (p.Glu4892Val)
c.14705A>T (p.Glu4902Val)
c.14621A>T (p.Glu4874Val)
19g.38585005G>ACA507246362RYR1c.1645G>A
c.3042G>A
c.3014G>A
n.102G>A
c.14709G>A (p.Glu4903=)
c.14694G>A (p.Glu4898=)
c.14691G>A (p.Glu4897=)
c.14676G>A (p.Glu4892=)
c.14706G>A (p.Glu4902=)
c.14622G>A (p.Glu4874=)
19g.38585005G>CCA061537RYR1c.1645G>C
c.3042G>C
c.3014G>C
n.102G>C
c.14709G>C (p.Glu4903Asp)
c.14694G>C (p.Glu4898Asp)
c.14691G>C (p.Glu4897Asp)
c.14676G>C (p.Glu4892Asp)
c.14706G>C (p.Glu4902Asp)
c.14622G>C (p.Glu4874Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.38585005G=CA2335094958RYR1c.1645G=
c.3042G=
c.3014G=
n.102G=
c.14709G= (p.Glu4903=)
c.14694G= (p.Glu4898=)
c.14691G= (p.Glu4897=)
c.14676G= (p.Glu4892=)
c.14706G= (p.Glu4902=)
c.14622G= (p.Glu4874=)

Number of alleles fetched