Variant ID: 3-197748344-G-A

NM_033029.3(LMLN):c.1393G>A;(p.Ala465Thr)

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: Ala465Thr
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.1393G>A p.Ala465Thr missense_variant 13/16 -
ENST00000332636.5 c.1237G>A p.Ala413Thr missense_variant 13/16 -
ENST00000420910.2 c.1504G>A p.Ala502Thr missense_variant 14/17 -
ENST00000451139.2 n.1995G>A - non_coding_transcript_exon_variant 13/16 -
ENST00000482695.1 c.1348G>A p.Ala450Thr missense_variant 14/17 -
NM_001136049.2 c.1504G>A p.Ala502Thr missense_variant 14/17 -
NM_033029.3 c.1393G>A p.Ala465Thr missense_variant 13/16 -
NR_026786.2 n.1388G>A - non_coding_transcript_exon_variant 14/17 -
NR_026787.2 n.1277G>A - non_coding_transcript_exon_variant 13/16 -