Variant ID: 3-197702954-CGA-TGG

NM_033029.3(LMLN):c.403_405delinsTGG;(p.Arg135Trp)

This variant was identified in 1 publication




Publications:


Three Nonsynonymous Single Nucleotide Polymorphisms in the RhitH Gene Cause Reduction of the Repression Activity That Leads to Upregulation of M-LPH, a Participant in Mitochondrial Function.

Bioresearch Open Access
R Iida, M Ueki, J Fujihara, H Takeshita, K Kimura-Kataoka, T Yasuda
Publication Date: 2013-12-01

Variant appearance in text: Msp: Arg135Trp
PubMed Link: 24380054
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000330198.4 c.403_405delinsTGG p.Arg135Trp missense_variant 4/16 -
ENST00000332636.5 c.247_249delinsTGG p.Arg83Trp missense_variant 4/16 -
ENST00000419117.1 c.187_189delinsTGG p.Arg63Trp missense_variant 4/6 -
ENST00000420910.2 c.403_405delinsTGG p.Arg135Trp missense_variant 4/17 -
ENST00000451139.2 n.408_410delinsTGG - non_coding_transcript_exon_variant 4/16 -
ENST00000482695.1 c.247_249delinsTGG p.Arg83Trp missense_variant 4/17 -
NM_001136049.2 c.403_405delinsTGG p.Arg135Trp missense_variant 4/17 -
NM_033029.3 c.403_405delinsTGG p.Arg135Trp missense_variant 4/16 -
NR_026786.2 n.287_289delinsTGG - non_coding_transcript_exon_variant 4/17 -
NR_026787.2 n.287_289delinsTGG - non_coding_transcript_exon_variant 4/16 -