Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.15642041G>ACA278201BTDc.383G>A (p.Arg128His)
n.1222G>A
c.149G>A (p.Arg50His)
c.443G>A (p.Arg148His)
c.449G>A (p.Arg150His)
c.161G>A (p.Arg54His)
n.518G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.15642041G=CA1347644971BTDc.383G= (p.Arg128=)
n.1222G=
c.149G= (p.Arg50=)
c.443G= (p.Arg148=)
c.449G= (p.Arg150=)
c.161G= (p.Arg54=)
n.518G=
dbSNP
3g.15642041G>TCA351605809BTDc.383G>T (p.Arg128Leu)
n.1222G>T
c.149G>T (p.Arg50Leu)
c.443G>T (p.Arg148Leu)
c.449G>T (p.Arg150Leu)
c.161G>T (p.Arg54Leu)
n.518G>T
dbSNP gnomAD v4
3g.15642041G>CCA351605808BTDc.383G>C (p.Arg128Pro)
n.1222G>C
c.149G>C (p.Arg50Pro)
c.443G>C (p.Arg148Pro)
c.449G>C (p.Arg150Pro)
c.161G>C (p.Arg54Pro)
n.518G>C
dbSNP gnomAD v4

Number of alleles fetched