DNA Alteration Details

System ID: 195

Gene: MLPH

Chromosome: 7

Variant Type: missense

Deleterious: no

Year Discovered: 2008

Is Defect?: No

Mode of Inheitance: Autosomal Recessive

Reference Sequence: GRCg6a

Variant Source: Naturally occurring variant

Genomic or Mitochondrial: g.4833305G>A

Coding DNA Sequence or Genomic DNA Sequence: c.103C>T

Protein Sequence: p.(R35W)

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Description: a genetic change or mutation in the coding DNA sequence of a gene, where a cytosine (C) nucleotide has been replaced by an thymine (T) at position 103, due to the mutation.

Trait: Color -> Feather: Unknown value

Breeds: NA