Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.67122013G>T | CA2098742564 | PCDH9 | c.3036+103392C>A (n.3036+103392C>A) | dbSNP |
13 | g.67122013G>A | CA251954064 | PCDH9 | c.3036+103392C>T (n.3036+103392C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.67122013G>C | CA700253525 | PCDH9 | c.3036+103392C>G (n.3036+103392C>G) | dbSNP |