Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_000018.4(ACADVL):c.139-1G>T | ACADVL | Likely pathogenic | 17 | 7123782 | 7123782 | G | T | criteria provided, single submitter | - |
Duplication | NM_000018.4(ACADVL):c.192dup (p.Pro65fs) | ACADVL | Likely pathogenic | 17 | 7123830 | 7123831 | G | GA | reviewed by expert panel | - |
Deletion | NM_000018.4(ACADVL):c.192del (p.Lys64fs) | ACADVL | Likely pathogenic | 17 | 7123831 | 7123831 | GA | G | reviewed by expert panel | - |
single nucleotide variant | NM_000018.4(ACADVL):c.199A>T (p.Lys67Ter) | ACADVL | Likely pathogenic | 17 | 7123843 | 7123843 | A | T | reviewed by expert panel | - |
single nucleotide variant | NM_000018.4(ACADVL):c.205-2A>G | ACADVL | Likely pathogenic | 17 | 7123921 | 7123921 | A | G | criteria provided, single submitter | - |
Duplication | NM_000018.4(ACADVL):c.210dup (p.Lys71Ter) | ACADVL | Likely pathogenic | 17 | 7123927 | 7123928 | C | CT | reviewed by expert panel | ClinGen:CA312282 |
single nucleotide variant | NM_000018.4(ACADVL):c.256C>T (p.Gln86Ter) | ACADVL | Likely pathogenic | 17 | 7123974 | 7123974 | C | T | criteria provided, single submitter | - |
Deletion | NM_000018.4(ACADVL):c.266del (p.Pro89fs) | ACADVL | Likely pathogenic | 17 | 7123982 | 7123982 | TC | T | reviewed by expert panel | - |
Deletion | NM_000018.4(ACADVL):c.277+1del | ACADVL | Likely pathogenic | 17 | 7123995 | 7123995 | CG | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000018.4(ACADVL):c.277+1G>T | ACADVL | Likely pathogenic | 17 | 7123996 | 7123996 | G | T | criteria provided, single submitter | ClinGen:CA16041858 |