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NM_001250.6(CD40):c.381C>T (p.Pro127=) AND not specified

Significance: Likely benign
ClinVar: RCV000589953

Variant: NM_001250.6(CD40):c.381C>T (p.Pro127=)

Type: Variant
Allele: NM_001250.6(CD40):c.381C>T (p.Pro127=) 487845
Gene:
Type: single nucleotide variant
Location: Chr20: 46122734 - assembly GRCh38
Chr20: 44751373 - assembly GRCh37
References: dbSNP: 763263083

Condition

Disease: not specified