Variant #0000443323 (NC_000003.11:g.128526468A>C, NM_004637.5:c.482A>C (RAB7A))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.128526468A>C
DNA change (hg38) g.128807625A>C
Published as -
ISCN -
DB-ID RAB7A_000003 See all 3 reported entries
Variant remarks expression cloning COS-7 cells, mis-localized to ER excl., increased protein stability/turnover
Reference PubMed: BasuRay 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner SIB - Livia Famiglietti
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-06-06 16:42:40 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB7A NM_004637.5 +/. ? c.482A>C r.(?) p.Asn161Thr


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