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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:
Type: single nucleotide variant
Location: Chr6: 76042019 - assembly GRCh38
Chr6: 76751736 - assembly GRCh37
References: dbSNP: 200651043

Condition

Disease: not provided