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NM_000101.4(CYBA):c.179A>C (p.Lys60Thr) AND not specified

Significance: Benign/Likely benign
ClinVar: RCV000239262

Variant: NM_000101.4(CYBA):c.179A>C (p.Lys60Thr)

Type: Variant
Allele: NM_000101.4(CYBA):c.179A>C (p.Lys60Thr) 247122
Gene:
Type: single nucleotide variant
Location: Chr16: 88713533 - assembly GRCh37
Chr16: 88647125 - assembly GRCh38
References: dbSNP: 11547387

Condition

Disease: not specified