single nucleotide variant | NM_000016.6(ACADM):c.387+1G>A | ACADM | Pathogenic | 1 | 76199314 | 76199314 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16040777 |
Duplication | NM_000016.6(ACADM):c.355dup (p.Val119fs) | ACADM | Pathogenic/Likely pathogenic | 1 | 76199277 | 76199278 | A | AG | criteria provided, multiple submitters, no conflicts | ClinGen:CA16617185 |
single nucleotide variant | NM_000016.6(ACADM):c.347G>A (p.Cys116Tyr) | ACADM | Pathogenic/Likely pathogenic | 1 | 76199273 | 76199273 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10576226,UniProtKB:P11310#VAR_015955 |
Deletion | NM_000016.6(ACADM):c.322_325del (p.Ile108fs) | ACADM | Pathogenic | 1 | 76199245 | 76199248 | TTTAA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA913064 |
single nucleotide variant | NM_000016.6(ACADM):c.287-1G>C | ACADM | Pathogenic | 1 | 76199212 | 76199212 | G | C | criteria provided, single submitter | ClinGen:CA275290 |
single nucleotide variant | NM_000016.6(ACADM):c.287-2A>G | ACADM | Likely pathogenic | 1 | 76199211 | 76199211 | A | G | criteria provided, single submitter | ClinGen:CA16043645 |
single nucleotide variant | NM_000016.6(ACADM):c.286+2T>G | ACADM | Likely pathogenic | 1 | 76198609 | 76198609 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000016.6(ACADM):c.253G>A (p.Gly85Ser) | ACADM | Likely pathogenic | 1 | 76198574 | 76198574 | G | A | criteria provided, single submitter | ClinGen:CA220176 |
single nucleotide variant | NM_000016.6(ACADM):c.250C>T (p.Leu84Phe) | ACADM | Pathogenic/Likely pathogenic | 1 | 76198571 | 76198571 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA913006 |
Duplication | NM_000016.6(ACADM):c.244dup (p.Trp82fs) | ACADM | Pathogenic | 1 | 76198564 | 76198565 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA274151 |