Variant #0000802260 (NC_000006.11:g.111632420T>C, NM_002912.3:c.8647A>G (REV3L))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111632420T>C
DNA change (hg38) -
Published as REV3L(NM_001286431.1):c.8413A>G (p.I2805V), REV3L(NM_002912.5):c.8647A>G (p.I2883V)
ISCN -
DB-ID REV3L_000041 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REV3L NM_002912.3 ?/. - c.8647A>G r.(?) p.(Ile2883Val)


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