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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
19
g.7170561T>G
CA403667101
INSR
c.1459A>C (p.Lys487Gln)
n.1434A>C
c.1537A>C (p.Lys513Gln)
ClinVar
dbSNP
19
g.7170561T>C
CA124213
INSR
c.1459A>G (p.Lys487Glu)
n.1434A>G
c.1537A>G (p.Lys513Glu)
ClinVar
dbSNP
gnomAD v3
gnomAD v4
Number of alleles fetched
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