Variant #0001056280 (NC_000018.9:g.12358857G>A, NM_006796.2:c.838C>T (AFG3L2))

Chromosome 18
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.12358857G>A
DNA change (hg38) -
Published as AFG3L2(NM_006796.2):c.838C>T (p.R280W), AFG3L2(NM_006796.3):c.838C>T (p.(Arg280Trp))
ISCN -
DB-ID AFG3L2_000054 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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFG3L2 NM_006796.2 ?/. - c.838C>T r.(?) p.(Arg280Trp)


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