Bibliome.ai browser hg19
Search
About
Stats
FAQ
SI c.844A>C ;(p.M282L)
Variant ID: 3-164781293-T-G
NM_001041.3(
SI
):c.844A>C;(p.M282L)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Single point mutations in ATP synthase compensate for mitochondrial genome loss in trypanosomes.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Dean, Samuel S; Gould, Matthew K MK; Dewar, Caroline E CE; Schnaufer, Achim C AC
Publication Date: 2013-09-03
Variant appearance in text: SI: M282L
PubMed Link:
23959897
Variant Present in the following documents:
Main text
View BVdb publication page