Variant #0000563961 (NC_000018.9:g.12377036G>A, NM_006796.2:c.46C>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.12377036G>A
DNA change (hg38) g.12377037G>A
Published as AFG3L2(NM_006796.2):c.46C>T (p.P16S), AFG3L2(NM_006796.3):c.46C>T (p.(Pro16Ser))
ISCN -
DB-ID AFG3L2_000057 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFG3L2 NM_006796.2 ?/. - c.46C>T r.(?) p.(Pro16Ser)


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