Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.44711547A>T | CA16602809 | B2M | n.83+107A>T c.1A>T (p.Met1Leu) n.61A>T n.56A>T | ClinVar dbSNP COSMIC COSMIC |
15 | g.44711547A>G | CA16602808 | B2M | n.83+107A>G c.1A>G (p.Met1Val) n.61A>G n.56A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
15 | g.44711547A= | CA2173753371 | B2M | n.83+107A= c.1A= (p.Met1=) n.61A= n.56A= | dbSNP |