Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.108580721G>C | CA258341 | COL4A5 | c.874G>C (p.Gly292Arg) c.550G>C (p.Gly184Arg) c.889G>C (p.Gly297Arg) | ClinVar dbSNP |
X | g.108580721G>A | CA413926389 | COL4A5 | c.874G>A (p.Gly292Arg) c.550G>A (p.Gly184Arg) c.889G>A (p.Gly297Arg) | ClinVar dbSNP |
X | g.108580721G= | CA2450683098 | COL4A5 | c.874G= (p.Gly292=) c.550G= (p.Gly184=) c.889G= (p.Gly297=) | dbSNP |