Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154532269C>TCA10566017G6PDc.1466G>A (p.Arg489His)
c.1376G>A (p.Arg459His)
c.1469G>A (p.Arg490His)
c.1379G>A (p.Arg460His)
c.1514G>A (p.Arg505His)
n.597G>A
dbSNP ExAC gnomAD
Xg.154532269C>ACA120979G6PDc.1466G>T (p.Arg489Leu)
c.1376G>T (p.Arg459Leu)
c.1469G>T (p.Arg490Leu)
c.1379G>T (p.Arg460Leu)
c.1514G>T (p.Arg505Leu)
n.597G>T
ClinVar dbSNP ExAC gnomAD
Xg.154532269C>GCA121060G6PDc.1466G>C (p.Arg489Pro)
c.1376G>C (p.Arg459Pro)
c.1469G>C (p.Arg490Pro)
c.1379G>C (p.Arg460Pro)
c.1514G>C (p.Arg505Pro)
n.597G>C
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched