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

Reference Sequence: GRCg6a

Variant Source: Naturally occurring variant

Genomic or Mitochondrial: g.1418711C>T

Coding DNA Sequence or Genomic DNA Sequence: c.172C>T

Protein Sequence: p.(Q58*)

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Description: a genetic change or mutation in the coding DNA sequence of a gene, where a cytosine (C) nucleotide has been replaced by a thymine (T) nucleotide at position 172.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