Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50627298_50627364delCA2697552823ARSAc.269_335del (p.Tyr90SerfsTer?)
c.11_77del (p.Tyr4SerfsTer?)
n.660_726del
ClinVar
22g.50627307G>ACA10325055ARSAc.324C>T (p.Thr108=)
c.66C>T (p.Thr22=)
n.715C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.50627307G>CCA515391549ARSAc.324C>G (p.Thr108=)
c.66C>G (p.Thr22=)
n.715C>G
gnomAD v4
22g.50627307G=CA2410959543ARSAc.324C= (p.Thr108=)
c.66C= (p.Thr22=)
n.715C=
22g.50627307G>TCA515391550ARSAc.324C>A (p.Thr108=)
c.66C>A (p.Thr22=)
n.715C>A
gnomAD v4
22g.50627308G>ACA412181209ARSAc.323C>T (p.Thr108Ile)
c.65C>T (p.Thr22Ile)
n.714C>T
ClinVar
22g.50627308G>CCA412181218ARSAc.323C>G (p.Thr108Ser)
c.65C>G (p.Thr22Ser)
n.714C>G
22g.50627308G>TCA412181222ARSAc.323C>A (p.Thr108Asn)
c.65C>A (p.Thr22Asn)
n.714C>A
22g.50627309T>ACA412181228ARSAc.322A>T (p.Thr108Ser)
c.64A>T (p.Thr22Ser)
n.713A>T
22g.50627309T>CCA412181231ARSAc.322A>G (p.Thr108Ala)
c.64A>G (p.Thr22Ala)
n.713A>G
22g.50627309T>GCA412181240ARSAc.322A>C (p.Thr108Pro)
c.64A>C (p.Thr22Pro)
n.713A>C
22g.50627310C>ACA515391551ARSAc.321G>T (p.Val107=)
c.63G>T (p.Val21=)
n.712G>T
gnomAD v4
22g.50627310C>GCA515391553ARSAc.321G>C (p.Val107=)
c.63G>C (p.Val21=)
n.712G>C
22g.50627310C>TCA515391552ARSAc.321G>A (p.Val107=)
c.63G>A (p.Val21=)
n.712G>A
22g.50627311A>CCA412181244ARSAc.320T>G (p.Val107Gly)
c.62T>G (p.Val21Gly)
n.711T>G
22g.50627311A>GCA412181260ARSAc.320T>C (p.Val107Ala)
c.62T>C (p.Val21Ala)
n.711T>C
22g.50627311A>TCA412181249ARSAc.320T>A (p.Val107Glu)
c.62T>A (p.Val21Glu)
n.711T>A
22g.50627312C>ACA412181265ARSAc.319G>T (p.Val107Leu)
c.61G>T (p.Val21Leu)
n.710G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.50627312C=CA2410959544ARSAc.319G= (p.Val107=)
c.61G= (p.Val21=)
n.710G=
22g.50627312C>GCA412181267ARSAc.319G>C (p.Val107Leu)
c.61G>C (p.Val21Leu)
n.710G>C
22g.50627312C>TCA412181266ARSAc.319G>A (p.Val107Met)
c.61G>A (p.Val21Met)
n.710G>A
gnomAD v4
22g.50627313C>ACA412181271ARSAc.318G>T (p.Glu106Asp)
c.60G>T (p.Glu20Asp)
n.709G>T
gnomAD v4
22g.50627313C=CA2410959545ARSAc.318G= (p.Glu106=)
c.60G= (p.Glu20=)
n.709G=
22g.50627313C>GCA412181277ARSAc.318G>C (p.Glu106Asp)
c.60G>C (p.Glu20Asp)
n.709G>C
22g.50627313C>TCA10325056ARSAc.318G>A (p.Glu106=)
c.60G>A (p.Glu20=)
n.709G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
22g.50627314T>ACA412181287ARSAc.317A>T (p.Glu106Val)
c.59A>T (p.Glu20Val)
n.708A>T
22g.50627314T>CCA412181289ARSAc.317A>G (p.Glu106Gly)
c.59A>G (p.Glu20Gly)
n.708A>G
gnomAD v4
22g.50627314T>GCA412181291ARSAc.317A>C (p.Glu106Ala)
c.59A>C (p.Glu20Ala)
n.708A>C
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

Number of alleles fetched