Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.197101667_197101671delCA1309369ASPMn.2108-5506_2108-5502del
c.7581_7585del (p.Tyr2527Ter)
c.4066-5506_4066-5502del (n.4066-5506_4066-5502del)
c.1816-5506_1816-5502del (n.1816-5506_1816-5502del)
c.1539_1543del (p.Tyr513Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
1g.197101671T>ACA344018383ASPMn.2108-5507A>T
c.7580A>T (p.Tyr2527Phe)
c.4066-5507A>T (n.4066-5507A>T)
c.1816-5507A>T (n.1816-5507A>T)
c.1538A>T (p.Tyr513Phe)
1g.197101671T>CCA35870621ASPMn.2108-5507A>G
c.7580A>G (p.Tyr2527Cys)
c.4066-5507A>G (n.4066-5507A>G)
c.1816-5507A>G (n.1816-5507A>G)
c.1538A>G (p.Tyr513Cys)
dbSNP
1g.197101671T>GCA1309370ASPMn.2108-5507A>C
c.7580A>C (p.Tyr2527Ser)
c.4066-5507A>C (n.4066-5507A>C)
c.1816-5507A>C (n.1816-5507A>C)
c.1538A>C (p.Tyr513Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.197101671T=CA1143885297ASPMn.2108-5507A=
c.7580A= (p.Tyr2527=)
c.4066-5507A= (n.4066-5507A=)
c.1816-5507A= (n.1816-5507A=)
c.1538A= (p.Tyr513=)
1g.197101672A=CA1217930023ASPMn.2108-5508T=
c.7579T= (p.Tyr2527=)
c.4066-5508T= (n.4066-5508T=)
c.1816-5508T= (n.1816-5508T=)
c.1537T= (p.Tyr513=)
1g.197101672A>CCA344018386ASPMn.2108-5508T>G
c.7579T>G (p.Tyr2527Asp)
c.4066-5508T>G (n.4066-5508T>G)
c.1816-5508T>G (n.1816-5508T>G)
c.1537T>G (p.Tyr513Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.197101672A>GCA344018387ASPMn.2108-5508T>C
c.7579T>C (p.Tyr2527His)
c.4066-5508T>C (n.4066-5508T>C)
c.1816-5508T>C (n.1816-5508T>C)
c.1537T>C (p.Tyr513His)
1g.197101672A>TCA344018388ASPMn.2108-5508T>A
c.7579T>A (p.Tyr2527Asn)
c.4066-5508T>A (n.4066-5508T>A)
c.1816-5508T>A (n.1816-5508T>A)
c.1537T>A (p.Tyr513Asn)
1g.197101673A=CA1217930024ASPMn.2108-5509T=
c.7578T= (p.Asn2526=)
c.4066-5509T= (n.4066-5509T=)
c.1816-5509T= (n.1816-5509T=)
c.1536T= (p.Asn512=)
1g.197101673A>CCA344018393ASPMn.2108-5509T>G
c.7578T>G (p.Asn2526Lys)
c.4066-5509T>G (n.4066-5509T>G)
c.1816-5509T>G (n.1816-5509T>G)
c.1536T>G (p.Asn512Lys)
1g.197101673A>GCA1309371ASPMn.2108-5509T>C
c.7578T>C (p.Asn2526=)
c.4066-5509T>C (n.4066-5509T>C)
c.1816-5509T>C (n.1816-5509T>C)
c.1536T>C (p.Asn512=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.197101673A>TCA344018390ASPMn.2108-5509T>A
c.7578T>A (p.Asn2526Lys)
c.4066-5509T>A (n.4066-5509T>A)
c.1816-5509T>A (n.1816-5509T>A)
c.1536T>A (p.Asn512Lys)
1g.197101674T>ACA344018395ASPMn.2108-5510A>T
c.7577A>T (p.Asn2526Ile)
c.4066-5510A>T (n.4066-5510A>T)
c.1816-5510A>T (n.1816-5510A>T)
c.1535A>T (p.Asn512Ile)
1g.197101674T>CCA344018397ASPMn.2108-5510A>G
c.7577A>G (p.Asn2526Ser)
c.4066-5510A>G (n.4066-5510A>G)
c.1816-5510A>G (n.1816-5510A>G)
c.1535A>G (p.Asn512Ser)
1g.197101674T>GCA344018398ASPMn.2108-5510A>C
c.7577A>C (p.Asn2526Thr)
c.4066-5510A>C (n.4066-5510A>C)
c.1816-5510A>C (n.1816-5510A>C)
c.1535A>C (p.Asn512Thr)
1g.197101675T>ACA344018401ASPMn.2108-5511A>T
c.7576A>T (p.Asn2526Tyr)
c.4066-5511A>T (n.4066-5511A>T)
c.1816-5511A>T (n.1816-5511A>T)
c.1534A>T (p.Asn512Tyr)
1g.197101675T>CCA171248ASPMn.2108-5511A>G
c.7576A>G (p.Asn2526Asp)
c.4066-5511A>G (n.4066-5511A>G)
c.1816-5511A>G (n.1816-5511A>G)
c.1534A>G (p.Asn512Asp)
ClinVar dbSNP
1g.197101675T>GCA344018403ASPMn.2108-5511A>C
c.7576A>C (p.Asn2526His)
c.4066-5511A>C (n.4066-5511A>C)
c.1816-5511A>C (n.1816-5511A>C)
c.1534A>C (p.Asn512His)
1g.197101675T=CA1148224851ASPMn.2108-5511A=
c.7576A= (p.Asn2526=)
c.4066-5511A= (n.4066-5511A=)
c.1816-5511A= (n.1816-5511A=)
c.1534A= (p.Asn512=)
1g.197101676T>ACA344018405ASPMn.2108-5512A>T
c.7575A>T (p.Glu2525Asp)
c.4066-5512A>T (n.4066-5512A>T)
c.1816-5512A>T (n.1816-5512A>T)
c.1533A>T (p.Glu511Asp)
1g.197101676T>CCA422805641ASPMn.2108-5512A>G
c.7575A>G (p.Glu2525=)
c.4066-5512A>G (n.4066-5512A>G)
c.1816-5512A>G (n.1816-5512A>G)
c.1533A>G (p.Glu511=)
dbSNP gnomAD v2 gnomAD v4
1g.197101676T>GCA344018407ASPMn.2108-5512A>C
c.7575A>C (p.Glu2525Asp)
c.4066-5512A>C (n.4066-5512A>C)
c.1816-5512A>C (n.1816-5512A>C)
c.1533A>C (p.Glu511Asp)
1g.197101676T=CA1217930026ASPMn.2108-5512A=
c.7575A= (p.Glu2525=)
c.4066-5512A= (n.4066-5512A=)
c.1816-5512A= (n.1816-5512A=)
c.1533A= (p.Glu511=)
1g.197101676_197101678delinsTTCCA1217930025ASPMn.2108-5514_2108-5512delinsGAA
c.7573_7575delinsGAA (p.Glu2525=)
c.4066-5514_4066-5512delinsGAA (n.4066-5514_4066-5512delinsGAA)
c.1816-5514_1816-5512delinsGAA (n.1816-5514_1816-5512delinsGAA)
c.1531_1533delinsGAA (p.Glu511=)
1g.197101677T>ACA344018409ASPMn.2108-5513A>T
c.7574A>T (p.Glu2525Val)
c.4066-5513A>T (n.4066-5513A>T)
c.1816-5513A>T (n.1816-5513A>T)
c.1532A>T (p.Glu511Val)
1g.197101677T>CCA344018411ASPMn.2108-5513A>G
c.7574A>G (p.Glu2525Gly)
c.4066-5513A>G (n.4066-5513A>G)
c.1816-5513A>G (n.1816-5513A>G)
c.1532A>G (p.Glu511Gly)
1g.197101677T>GCA344018413ASPMn.2108-5513A>C
c.7574A>C (p.Glu2525Ala)
c.4066-5513A>C (n.4066-5513A>C)
c.1816-5513A>C (n.1816-5513A>C)
c.1532A>C (p.Glu511Ala)
1g.197101680_197101681delCA16609502ASPMn.2108-5514_2108-5513del
c.7573_7574del (p.Glu2525LysfsTer17)
c.4066-5514_4066-5513del (n.4066-5514_4066-5513del)
c.1816-5514_1816-5513del (n.1816-5514_1816-5513del)
c.1531_1532del (p.Glu511LysfsTer17)
ClinVar dbSNP
1g.197101678C>ACA344018415ASPMn.2108-5514G>T
c.7573G>T (p.Glu2525Ter)
c.4066-5514G>T (n.4066-5514G>T)
c.1816-5514G>T (n.1816-5514G>T)
c.1531G>T (p.Glu511Ter)
1g.197101678C=CA1217930027ASPMn.2108-5514G=
c.7573G= (p.Glu2525=)
c.4066-5514G= (n.4066-5514G=)
c.1816-5514G= (n.1816-5514G=)
c.1531G= (p.Glu511=)
1g.197101678C>GCA1309372ASPMn.2108-5514G>C
c.7573G>C (p.Glu2525Gln)
c.4066-5514G>C (n.4066-5514G>C)
c.1816-5514G>C (n.1816-5514G>C)
c.1531G>C (p.Glu511Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
1g.197101678C>TCA344018417ASPMn.2108-5514G>A
c.7573G>A (p.Glu2525Lys)
c.4066-5514G>A (n.4066-5514G>A)
c.1816-5514G>A (n.1816-5514G>A)
c.1531G>A (p.Glu511Lys)
gnomAD v4
1g.197101679T>ACA344018419ASPMn.2108-5515A>T
c.7572A>T (p.Arg2524Ser)
c.4066-5515A>T (n.4066-5515A>T)
c.1816-5515A>T (n.1816-5515A>T)
c.1530A>T (p.Arg510Ser)
1g.197101679T>CCA422805645ASPMn.2108-5515A>G
c.7572A>G (p.Arg2524=)
c.4066-5515A>G (n.4066-5515A>G)
c.1816-5515A>G (n.1816-5515A>G)
c.1530A>G (p.Arg510=)
1g.197101679T>GCA344018421ASPMn.2108-5515A>C
c.7572A>C (p.Arg2524Ser)
c.4066-5515A>C (n.4066-5515A>C)
c.1816-5515A>C (n.1816-5515A>C)
c.1530A>C (p.Arg510Ser)
1g.197101680C>ACA344018423ASPMn.2108-5516G>T
c.7571G>T (p.Arg2524Ile)
c.4066-5516G>T (n.4066-5516G>T)
c.1816-5516G>T (n.1816-5516G>T)
c.1529G>T (p.Arg510Ile)
1g.197101680C>GCA344018425ASPMn.2108-5516G>C
c.7571G>C (p.Arg2524Thr)
c.4066-5516G>C (n.4066-5516G>C)
c.1816-5516G>C (n.1816-5516G>C)
c.1529G>C (p.Arg510Thr)
gnomAD v4
1g.197101680C>TCA344018427ASPMn.2108-5516G>A
c.7571G>A (p.Arg2524Lys)
c.4066-5516G>A (n.4066-5516G>A)
c.1816-5516G>A (n.1816-5516G>A)
c.1529G>A (p.Arg510Lys)
gnomAD v4
1g.197101681T>ACA344018428ASPMn.2108-5517A>T
c.7570A>T (p.Arg2524Ter)
c.4066-5517A>T (n.4066-5517A>T)
c.1816-5517A>T (n.1816-5517A>T)
c.1528A>T (p.Arg510Ter)
1g.197101681T>CCA344018429ASPMn.2108-5517A>G
c.7570A>G (p.Arg2524Gly)
c.4066-5517A>G (n.4066-5517A>G)
c.1816-5517A>G (n.1816-5517A>G)
c.1528A>G (p.Arg510Gly)
1g.197101681T>GCA422805649ASPMn.2108-5517A>C
c.7570A>C (p.Arg2524=)
c.4066-5517A>C (n.4066-5517A>C)
c.1816-5517A>C (n.1816-5517A>C)
c.1528A>C (p.Arg510=)
1g.197101682_197101683delCA2586967836ASPMn.2108-5518_2108-5517del
c.7569_7570del (p.Glu2525LysfsTer17)
c.4066-5518_4066-5517del (n.4066-5518_4066-5517del)
c.1816-5518_1816-5517del (n.1816-5518_1816-5517del)
c.1527_1528del (p.Glu511LysfsTer17)
1g.197101682T>ACA344018430ASPMn.2108-5518A>T
c.7569A>T (p.Gln2523His)
c.4066-5518A>T (n.4066-5518A>T)
c.1816-5518A>T (n.1816-5518A>T)
c.1527A>T (p.Gln509His)
1g.197101682T>CCA1309373ASPMn.2108-5518A>G
c.7569A>G (p.Gln2523=)
c.4066-5518A>G (n.4066-5518A>G)
c.1816-5518A>G (n.1816-5518A>G)
c.1527A>G (p.Gln509=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.197101682T>GCA344018433ASPMn.2108-5518A>C
c.7569A>C (p.Gln2523His)
c.4066-5518A>C (n.4066-5518A>C)
c.1816-5518A>C (n.1816-5518A>C)
c.1527A>C (p.Gln509His)
1g.197101682T=CA1142244251ASPMn.2108-5518A=
c.7569A= (p.Gln2523=)
c.4066-5518A= (n.4066-5518A=)
c.1816-5518A= (n.1816-5518A=)
c.1527A= (p.Gln509=)
1g.197101683T>ACA344018435ASPMn.2108-5519A>T
c.7568A>T (p.Gln2523Leu)
c.4066-5519A>T (n.4066-5519A>T)
c.1816-5519A>T (n.1816-5519A>T)
c.1526A>T (p.Gln509Leu)
1g.197101683T>CCA1309374ASPMn.2108-5519A>G
c.7568A>G (p.Gln2523Arg)
c.4066-5519A>G (n.4066-5519A>G)
c.1816-5519A>G (n.1816-5519A>G)
c.1526A>G (p.Gln509Arg)
dbSNP ExAC gnomAD v3 gnomAD v4
1g.197101683T>GCA344018436ASPMn.2108-5519A>C
c.7568A>C (p.Gln2523Pro)
c.4066-5519A>C (n.4066-5519A>C)
c.1816-5519A>C (n.1816-5519A>C)
c.1526A>C (p.Gln509Pro)

Number of alleles fetched