Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.27126417G>T | CA191284042 | TEK | c.52+16775G>T (n.52+16775G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.27126417G>C | CA1841962999 | TEK | c.52+16775G>C (n.52+16775G>C) | dbSNP |
9 | g.27126417G= | CA1841962998 | TEK | c.52+16775G= (n.52+16775G=) | dbSNP |