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

Reference Sequence:

Variant Source: Naturally occurring variant

Genomic or Mitochondrial:

Coding DNA Sequence or Genomic DNA Sequence: c.G>C

Protein Sequence: p.(C125S)

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Description: a genetic change or mutation in the coding DNA sequence of a gene, where a guanine (g) nucleotide has been replaced by a cytosine (C) nucleotide at a specific position.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