DNA Alteration Details
System ID: 177
Gene: TNFRSF10B
Chromosome: 22
Variant Type: missense
Deleterious: no
Year Discovered: 2002
Is Defect?: Unknown
Mode of Inheitance: Autosomal Recessive
Variant Source: Naturally occurring variant
Reference Website: Visit website
Verbal Description: a genetic change or mutation in the coding DNA sequence of a gene, where a guanine (g) nucleotide has been replaced by a cytosine (C) nucleotide at a specific position.
Trait: Blood: subgroup B
Breeds:
NA