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NM_001614.5(ACTG1):c.177G>A (p.Gln59=) AND not specified

Significance: Benign
ClinVar: RCV000037122

Variant: NM_001614.5(ACTG1):c.177G>A (p.Gln59=)

Type: Variant
Allele: NM_001614.5(ACTG1):c.177G>A (p.Gln59=) 53314
Gene:
Type: single nucleotide variant
Location: Chr17: 81512089 - assembly GRCh38
Chr17: 79479115 - assembly GRCh37
References: dbSNP: 11549220

Condition

Disease: not specified