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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.108578120G>C
CA413923925
COL4A5
c.687+1G>C (n.687+1G>C)
c.363+1G>C (n.363+1G>C)
c.702+1G>C (n.702+1G>C)
ClinVar
dbSNP
X
g.108578120G>A
CA258310
COL4A5
c.687+1G>A (n.687+1G>A)
c.363+1G>A (n.363+1G>A)
c.702+1G>A (n.702+1G>A)
ClinVar
dbSNP
Number of alleles fetched
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