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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.2160825G>A
CA5818186
INS,INS-IGF2
c.147C>T (p.Phe49=)
n.206C>T
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
11
g.2160825G>C
CA123073
INS,INS-IGF2
c.147C>G (p.Phe49Leu)
n.206C>G
ClinVar
dbSNP
gnomAD v4
Number of alleles fetched
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