DNA Alteration Details
System ID: 179
Gene: TNFRSF10B
Chromosome: 22
Variant Type: nonsense (stop-gain)
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Description: a genetic change or mutation in the coding DNA sequence of a gene, where a cytosine (C) nucleotide has been replaced by a thymine (T) nucleotide at position 172.
Trait: Blood: subgroup B
Breeds:
NA