Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_015506.3(MMACHC):c.347T>C (p.Leu116Pro) | MMACHC | Pathogenic/Likely pathogenic | 1 | 45973954 | 45973954 | T | C | criteria provided, multiple submitters, no conflicts | OMIM:609831.0002,ClinGen:CA251786,UniProtKB:Q9Y4U1#VAR_024771 |