Variant ID: 3-197765476-T-C

NM_033029.3(LMLN):c.1906T>C;(p.Trp636Arg)

This variant was identified in 1 publication




Publications:


Genetic disorders in beef cattle: a review.

Genes & Genomics
A Ciepłoch, K Rutkowska, J Oprządek, E Poławska
Publication Date: 2017

Variant appearance in text: Msp: 1906T>C
PubMed Link: 28458779
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000330198.4 c.1906T>C p.Trp636Arg missense_variant 16/16 -
ENST00000332636.5 c.1750T>C p.Trp584Arg missense_variant 16/16 -
ENST00000420910.2 c.2017T>C p.Trp673Arg missense_variant 17/17 -
ENST00000423460.1 n.258A>G - non_coding_transcript_exon_variant 3/3 -
ENST00000451139.2 n.2508T>C - non_coding_transcript_exon_variant 16/16 -
ENST00000482695.1 c.1861T>C p.Trp621Arg missense_variant 17/17 -
NM_001136049.2 c.2017T>C p.Trp673Arg missense_variant 17/17 -
NM_033029.3 c.1906T>C p.Trp636Arg missense_variant 16/16 -
NR_026786.2 n.1901T>C - non_coding_transcript_exon_variant 17/17 -
NR_026787.2 n.1790T>C - non_coding_transcript_exon_variant 16/16 -
NR_046669.1 n.267A>G - non_coding_transcript_exon_variant 4/4 -