NM_001563.4(IMPG1):c.175C>T (p.Arg59Ter) AND not provided
| Significance: | Likely pathogenic |
|---|---|
| ClinVar: | RCV000760627 |
Variant: NM_001563.4(IMPG1):c.175C>T (p.Arg59Ter) |
|
| Type: | Variant |
Allele: NM_001563.4(IMPG1):c.175C>T (p.Arg59Ter) 611665 |
|
| Gene: | IMPG1 |
| Type: | single nucleotide variant |
| Location: |
Chr6: 76042019
- assembly
GRCh38 Chr6: 76751736 - assembly GRCh37 |
| References: | dbSNP:
200651043 |
Condition |
|
| Disease: | not provided |