Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.102872397G>ACA7041760BIVM-ERCC5,ERCC5n.3119G>A
n.3527G>A
n.3655G>A
n.2248G>A
c.3553G>A (p.Glu1185Lys)
c.4240G>A (p.Glu1414Lys)
c.*2639G>A (n.*2639G>A)
n.3007G>A
n.3246G>A
n.2362G>A
c.*50G>A (n.*50G>A)
c.2878G>A (p.Glu960Lys)
c.2374G>A (p.Glu792Lys)
c.577G>A (p.Glu193Lys)
c.4154G>A
c.2875G>A (p.Glu959Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
13g.102872397G>TCA257525BIVM-ERCC5,ERCC5n.3119G>T
n.3527G>T
n.3655G>T
n.2248G>T
c.3553G>T (p.Glu1185Ter)
c.4240G>T (p.Glu1414Ter)
c.*2639G>T (n.*2639G>T)
n.3007G>T
n.3246G>T
n.2362G>T
c.*50G>T (n.*50G>T)
c.2878G>T (p.Glu960Ter)
c.2374G>T (p.Glu792Ter)
c.577G>T (p.Glu193Ter)
c.4154G>T
c.2875G>T (p.Glu959Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched