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.25013164T>ACA515947477ARXc.831A>T (p.Ala277=)
Xg.25013164T>CCA515947481ARXc.831A>G (p.Ala277=)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.25013164T>GCA515947482ARXc.831A>C (p.Ala277=)
Xg.25013164T=CA2420209135ARXc.831A= (p.Ala277=)
Xg.25013165G>ACA412612347ARXc.830C>T (p.Ala277Val)
Xg.25013165G>CCA412612348ARXc.830C>G (p.Ala277Gly)
Xg.25013165G>TCA412612349ARXc.830C>A (p.Ala277Glu)
Xg.25013166C>ACA412612350ARXc.829G>T (p.Ala277Ser)
Xg.25013166C=CA2420209136ARXc.829G= (p.Ala277=)
Xg.25013166C>GCA412612351ARXc.829G>C (p.Ala277Pro)
Xg.25013166C>TCA412612352ARXc.829G>A (p.Ala277Thr)
dbSNP gnomAD v2 gnomAD v4
Xg.25013167T>ACA515947495ARXc.828A>T (p.Ala276=)
Xg.25013167T>CCA515947496ARXc.828A>G (p.Ala276=)
Xg.25013167T>GCA515947497ARXc.828A>C (p.Ala276=)
Xg.25013168delCA2552618203ARXc.827del (p.Ala276GlufsTer?)
Xg.25013168G>ACA412612354ARXc.827C>T (p.Ala276Val)
Xg.25013168G>CCA412612355ARXc.827C>G (p.Ala276Gly)
Xg.25013168G>TCA412612353ARXc.827C>A (p.Ala276Glu)
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.25013169C>ACA412612356ARXc.826G>T (p.Ala276Ser)
dbSNP gnomAD v2 gnomAD v4
Xg.25013169C=CA2420209137ARXc.826G= (p.Ala276=)
Xg.25013169C>GCA412612357ARXc.826G>C (p.Ala276Pro)
dbSNP gnomAD v4
Xg.25013169C>TCA412612358ARXc.826G>A (p.Ala276Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013170G>ACA16616649ARXc.825C>T (p.Ala275=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013170G>CCA515947502ARXc.825C>G (p.Ala275=)
Xg.25013170G=CA2420209138ARXc.825C= (p.Ala275=)
Xg.25013170G>TCA515947505ARXc.825C>A (p.Ala275=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.25013170_25013171delCA2530386685ARXc.824_825del (p.Ala275GlyfsTer28)
Xg.25013171G>ACA412612359ARXc.824C>T (p.Ala275Val)
dbSNP gnomAD v4
Xg.25013171G>CCA412612360ARXc.824C>G (p.Ala275Gly)
Xg.25013171G>TCA412612361ARXc.824C>A (p.Ala275Asp)
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)

Number of alleles fetched