Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.89776598G>C | CA274596800 | MESP2 | c.241G>C (p.Gly81Arg) n.39-1467G>C c.31-1467G>C (n.31-1467G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.89776598G>T | CA343154 | MESP2 | c.241G>T (p.Gly81Ter) n.39-1467G>T c.31-1467G>T (n.31-1467G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.89776598G>A | CA393769372 | MESP2 | c.241G>A (p.Gly81Arg) n.39-1467G>A c.31-1467G>A (n.31-1467G>A) | dbSNP gnomAD v2 gnomAD v4 |