Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_015702.3(MMADHC):c.776T>C (p.Leu259Pro) | MMADHC | Likely pathogenic | 2 | 150426603 | 150426603 | A | G | criteria provided, single submitter | ClinGen:CA114486,UniProtKB:Q9H3L0#VAR_043847,OMIM:611935.0001 |