Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012021_25015415delCA915950806ARXc.196+129_1073+903del
ClinVar
Xg.25013161_25013190delCA2693353413ARXc.810_839del (p.Thr271_Ala280del)
gnomAD v4
Xg.25013176_25013193dupCA2693353440ARXc.810_827dup (p.Ala276_Ala277insThrGlyAlaValAlaAla)
gnomAD v4
Xg.25013176_25013193delCA2592314635ARXc.810_827del (p.Thr271_Ala276del)
gnomAD v3 gnomAD v4
Xg.25013172C>ACA412612364ARXc.823G>T (p.Ala275Ser)
Xg.25013172C>GCA412612362ARXc.823G>C (p.Ala275Pro)
Xg.25013172C>TCA412612363ARXc.823G>A (p.Ala275Thr)
gnomAD v4
Xg.25013173C>ACA515947510ARXc.822G>T (p.Val274=)
gnomAD v4
Xg.25013173C=CA2420209139ARXc.822G= (p.Val274=)
Xg.25013173C>GCA515947511ARXc.822G>C (p.Val274=)
Xg.25013173C>TCA515947512ARXc.822G>A (p.Val274=)
ClinVar dbSNP
Xg.25013174A=CA2420209140ARXc.821T= (p.Val274=)
Xg.25013174A>CCA412612365ARXc.821T>G (p.Val274Gly)
Xg.25013174A>GCA10373874ARXc.821T>C (p.Val274Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013174A>TCA412612366ARXc.821T>A (p.Val274Glu)
Xg.25013174dupCA2580618167ARXc.821dup (p.Ala275GlyfsTer29)
ClinVar
Xg.25013174_25013176delCA2563881402ARXc.819_821del (p.Val274del)
Xg.25013175C>ACA412612367ARXc.820G>T (p.Val274Leu)
gnomAD v4
Xg.25013175C>GCA412612368ARXc.820G>C (p.Val274Leu)
Xg.25013175C>TCA412612369ARXc.820G>A (p.Val274Met)
Xg.25013176G>ACA515947517ARXc.819C>T (p.Ala273=)
dbSNP
Xg.25013176G>CCA515947521ARXc.819C>G (p.Ala273=)
Xg.25013176G=CA2420209141ARXc.819C= (p.Ala273=)
Xg.25013176G>TCA515947522ARXc.819C>A (p.Ala273=)
gnomAD v4
Xg.25013177G>ACA412612370ARXc.818C>T (p.Ala273Val)
gnomAD v4
Xg.25013177G>CCA327733043ARXc.818C>G (p.Ala273Gly)
dbSNP gnomAD v4
Xg.25013177G=CA2420209142ARXc.818C= (p.Ala273=)
Xg.25013177G>TCA412612371ARXc.818C>A (p.Ala273Asp)
gnomAD v4
Xg.25013178C>ACA412612372ARXc.817G>T (p.Ala273Ser)
gnomAD v4
Xg.25013178C=CA2420209143ARXc.817G= (p.Ala273=)
Xg.25013178C>GCA412612373ARXc.817G>C (p.Ala273Pro)
dbSNP gnomAD v2 gnomAD v4
Xg.25013178C>TCA412612374ARXc.817G>A (p.Ala273Thr)
gnomAD v4
Xg.25013179G>ACA515947528ARXc.816C>T (p.Gly272=)
ClinVar gnomAD v4 COSMIC
Xg.25013179G>CCA515947529ARXc.816C>G (p.Gly272=)
Xg.25013179G>TCA515947531ARXc.816C>A (p.Gly272=)
gnomAD v4
Xg.25013180C>ACA10373875ARXc.815G>T (p.Gly272Val)
dbSNP ExAC
Xg.25013180C=CA2420209144ARXc.815G= (p.Gly272=)
Xg.25013180C>GCA412612375ARXc.815G>C (p.Gly272Ala)
Xg.25013180C>TCA412612376ARXc.815G>A (p.Gly272Asp)
dbSNP gnomAD v2 gnomAD v4
Xg.25013181C>ACA412612377ARXc.814G>T (p.Gly272Cys)
gnomAD v4
Xg.25013181C>GCA412612378ARXc.814G>C (p.Gly272Arg)
Xg.25013181C>TCA412612379ARXc.814G>A (p.Gly272Ser)
gnomAD v4
Xg.25013182A=CA2420209145ARXc.813T= (p.Thr271=)
Xg.25013182A>CCA515947549ARXc.813T>G (p.Thr271=)
Xg.25013182A>GCA515947548ARXc.813T>C (p.Thr271=)
ClinVar dbSNP gnomAD v4
Xg.25013182A>TCA515947546ARXc.813T>A (p.Thr271=)
Xg.25013182_25013189delCA2557346376ARXc.806_813del (p.Ala269GlyfsTer?)
Xg.25013183G>ACA412612380ARXc.812C>T (p.Thr271Ile)
Xg.25013183G>CCA412612381ARXc.812C>G (p.Thr271Ser)
Xg.25013183G>TCA412612382ARXc.812C>A (p.Thr271Asn)
gnomAD v4

Number of alleles fetched