Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50627298_50627364delCA2697552823ARSAc.269_335del (p.Tyr90SerfsTer?)
c.11_77del (p.Tyr4SerfsTer?)
n.660_726del
ClinVar
22g.50627315C>ACA412181292ARSAc.316G>T (p.Glu106Ter)
c.58G>T (p.Glu20Ter)
n.707G>T
gnomAD v4
22g.50627315C>GCA412181293ARSAc.316G>C (p.Glu106Gln)
c.58G>C (p.Glu20Gln)
n.707G>C
22g.50627315C>TCA412181297ARSAc.316G>A (p.Glu106Lys)
c.58G>A (p.Glu20Lys)
n.707G>A
gnomAD v4
22g.50627316C>ACA412181301ARSAc.315G>T (p.Glu105Asp)
c.57G>T (p.Glu19Asp)
n.706G>T
22g.50627316C>GCA412181303ARSAc.315G>C (p.Glu105Asp)
c.57G>C (p.Glu19Asp)
n.706G>C
22g.50627316C>TCA515391554ARSAc.315G>A (p.Glu105=)
c.57G>A (p.Glu19=)
n.706G>A
22g.50627317T>ACA412181316ARSAc.314A>T (p.Glu105Val)
c.56A>T (p.Glu19Val)
n.705A>T
22g.50627317T>CCA412181315ARSAc.314A>G (p.Glu105Gly)
c.56A>G (p.Glu19Gly)
n.705A>G
gnomAD v4
22g.50627317T>GCA412181311ARSAc.314A>C (p.Glu105Ala)
c.56A>C (p.Glu19Ala)
n.705A>C
22g.50627318C>ACA412181317ARSAc.313G>T (p.Glu105Ter)
c.55G>T (p.Glu19Ter)
n.704G>T
gnomAD v4
22g.50627318C>GCA412181318ARSAc.313G>C (p.Glu105Gln)
c.55G>C (p.Glu19Gln)
n.704G>C
22g.50627318C>TCA412181320ARSAc.313G>A (p.Glu105Lys)
c.55G>A (p.Glu19Lys)
n.704G>A
22g.50627319C>ACA515391555ARSAc.312G>T (p.Leu104=)
c.54G>T (p.Leu18=)
n.703G>T
22g.50627319C>GCA515391556ARSAc.312G>C (p.Leu104=)
c.54G>C (p.Leu18=)
n.703G>C
22g.50627319C>TCA515391557ARSAc.312G>A (p.Leu104=)
c.54G>A (p.Leu18=)
n.703G>A
ClinVar
22g.50627320delCA2580099998ARSAc.311del (p.Leu104ArgfsTer4)
c.53del (p.Leu18ArgfsTer4)
n.702del
ClinVar
22g.50627320A=CA2410959546ARSAc.311T= (p.Leu104=)
c.53T= (p.Leu18=)
n.702T=
22g.50627320A>CCA412181321ARSAc.311T>G (p.Leu104Arg)
c.53T>G (p.Leu18Arg)
n.702T>G
gnomAD v4
22g.50627320A>GCA325531593ARSAc.311T>C (p.Leu104Pro)
c.53T>C (p.Leu18Pro)
n.702T>C
dbSNP gnomAD v4
22g.50627320A>TCA412181340ARSAc.311T>A (p.Leu104Gln)
c.53T>A (p.Leu18Gln)
n.702T>A
gnomAD v4
22g.50627321G>ACA515391558ARSAc.310C>T (p.Leu104=)
c.52C>T (p.Leu18=)
n.701C>T
ClinVar dbSNP gnomAD v4
22g.50627321G>CCA412181348ARSAc.310C>G (p.Leu104Val)
c.52C>G (p.Leu18Val)
n.701C>G
22g.50627321G>TCA412181351ARSAc.310C>A (p.Leu104Met)
c.52C>A (p.Leu18Met)
n.701C>A
gnomAD v4
22g.50627324delCA2657593945ARSAc.310del (p.Leu104TrpfsTer4)
c.52del (p.Leu18TrpfsTer4)
n.701del
gnomAD v4
22g.50627322G>ACA10325057ARSAc.309C>T (p.Pro103=)
c.51C>T (p.Pro17=)
n.700C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
22g.50627322G>CCA515391559ARSAc.309C>G (p.Pro103=)
c.51C>G (p.Pro17=)
n.700C>G
22g.50627322G=CA2410959547ARSAc.309C= (p.Pro103=)
c.51C= (p.Pro17=)
n.700C=
22g.50627322G>TCA515391560ARSAc.309C>A (p.Pro103=)
c.51C>A (p.Pro17=)
n.700C>A
22g.50627323G>ACA412181367ARSAc.308C>T (p.Pro103Leu)
c.50C>T (p.Pro17Leu)
n.699C>T
gnomAD v4
22g.50627323G>CCA412181375ARSAc.308C>G (p.Pro103Arg)
c.50C>G (p.Pro17Arg)
n.699C>G
ClinVar
22g.50627323G>TCA412181378ARSAc.308C>A (p.Pro103His)
c.50C>A (p.Pro17His)
n.699C>A
gnomAD v4
22g.50627324G>ACA412181390ARSAc.307C>T (p.Pro103Ser)
c.49C>T (p.Pro17Ser)
n.698C>T
gnomAD v4
22g.50627324G>CCA412181386ARSAc.307C>G (p.Pro103Ala)
c.49C>G (p.Pro17Ala)
n.698C>G
22g.50627324G>TCA412181383ARSAc.307C>A (p.Pro103Thr)
c.49C>A (p.Pro17Thr)
n.698C>A
gnomAD v4
22g.50627325C>ACA515391561ARSAc.306G>T (p.Leu102=)
c.48G>T (p.Leu16=)
n.697G>T
ClinVar dbSNP gnomAD v4
22g.50627325C=CA2410959548ARSAc.306G= (p.Leu102=)
c.48G= (p.Leu16=)
n.697G=
22g.50627325C>GCA515391562ARSAc.306G>C (p.Leu102=)
c.48G>C (p.Leu16=)
n.697G>C
22g.50627325C>TCA10325058ARSAc.306G>A (p.Leu102=)
c.48G>A (p.Leu16=)
n.697G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50627326A>CCA412181392ARSAc.305T>G (p.Leu102Arg)
c.47T>G (p.Leu16Arg)
n.696T>G
22g.50627326A>GCA412181395ARSAc.305T>C (p.Leu102Pro)
c.47T>C (p.Leu16Pro)
n.696T>C
gnomAD v4
22g.50627326A>TCA412181396ARSAc.305T>A (p.Leu102Gln)
c.47T>A (p.Leu16Gln)
n.696T>A
22g.50627326_50627327delinsAGCA2410959549ARSAc.304_305delinsCT (p.Leu102=)
c.46_47delinsCT (p.Leu16=)
n.695_696delinsCT
22g.50627327G>ACA515391563ARSAc.304C>T (p.Leu102=)
c.46C>T (p.Leu16=)
n.695C>T
gnomAD v4
22g.50627327G>CCA412181399ARSAc.304C>G (p.Leu102Val)
c.46C>G (p.Leu16Val)
n.695C>G
22g.50627327G>TCA412181401ARSAc.304C>A (p.Leu102Met)
c.46C>A (p.Leu16Met)
n.695C>A
gnomAD v4
22g.50627328delCA278486ARSAc.304del (p.Leu102CysfsTer6)
c.46del (p.Leu16CysfsTer6)
n.695del
ClinVar dbSNP gnomAD v4
22g.50627328G>ACA10325061ARSAc.303C>T (p.Gly101=)
c.45C>T (p.Gly15=)
n.694C>T
dbSNP ExAC gnomAD v2 gnomAD v4
22g.50627328G>CCA515391565ARSAc.303C>G (p.Gly101=)
c.45C>G (p.Gly15=)
n.694C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
22g.50627328G=CA2410959551ARSAc.303C= (p.Gly101=)
c.45C= (p.Gly15=)
n.694C=

Number of alleles fetched