Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.127426227G>CCA114416PROCc.678G>C (p.Gln226His)
c.121-2130G>C
c.780G>C (p.Gln260His)
n.264G>C
c.861G>C (p.Gln287His)
c.843G>C (p.Gln281His)
c.741G>C (p.Gln247His)
c.921G>C (p.Gln307His)
c.1023G>C (p.Gln341His)
c.963G>C (p.Gln321His)
n.4358C>G
c.846G>C (p.Gln282His)
c.864G>C (p.Gln288His)
c.621G>C (p.Gln207His)
c.654G>C (p.Gln218His)
c.672G>C (p.Gln224His)
ClinVar dbSNP
2g.127426227G>ACA428618368PROCc.678G>A (p.Gln226=)
c.121-2130G>A
c.780G>A (p.Gln260=)
n.264G>A
c.861G>A (p.Gln287=)
c.843G>A (p.Gln281=)
c.741G>A (p.Gln247=)
c.921G>A (p.Gln307=)
c.1023G>A (p.Gln341=)
c.963G>A (p.Gln321=)
n.4358C>T
c.846G>A (p.Gln282=)
c.864G>A (p.Gln288=)
c.621G>A (p.Gln207=)
c.654G>A (p.Gln218=)
c.672G>A (p.Gln224=)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.127426227G=CA1286883461PROCc.678G= (p.Gln226=)
c.121-2130G=
c.780G= (p.Gln260=)
n.264G=
c.861G= (p.Gln287=)
c.843G= (p.Gln281=)
c.741G= (p.Gln247=)
c.921G= (p.Gln307=)
c.1023G= (p.Gln341=)
c.963G= (p.Gln321=)
n.4358C=
c.846G= (p.Gln282=)
c.864G= (p.Gln288=)
c.621G= (p.Gln207=)
c.654G= (p.Gln218=)
c.672G= (p.Gln224=)
dbSNP

Number of alleles fetched