Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.230704350T>ACA1448119AGTc.1098-13A>T (p.=)
c.*557-13A>T (p.=)
n.5403-13A>T
c.829+5645A>T (p.=)
n.3191A>T
c.*592-13A>T (p.=)
c.1125-13A>T (p.=)
dbSNP ExAC gnomAD
1g.230704350T>CCA1448117AGTc.1098-13A>G (p.=)
c.*557-13A>G (p.=)
n.5403-13A>G
c.829+5645A>G (p.=)
n.3191A>G
c.*592-13A>G (p.=)
c.1125-13A>G (p.=)
ClinVar dbSNP ExAC gnomAD
1g.230704350T>GCA1448118AGTc.1098-13A>C (p.=)
c.*557-13A>C (p.=)
n.5403-13A>C
c.829+5645A>C (p.=)
n.3191A>C
c.*592-13A>C (p.=)
c.1125-13A>C (p.=)
dbSNP ExAC gnomAD

Number of alleles fetched