Variant #0000502767 (NC_000001.10:g.12049344A>G, NM_014874.3:c.119A>G (MFN2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12049344A>G
DNA change (hg38) g.11989287A>G
Published as MFN2(NM_014874.3):c.119A>G (p.N40S), MFN2(NM_014874.4):c.119A>G (p.(Asn40Ser))
ISCN -
DB-ID MFN2_000160 See all 3 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) 1.0E-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 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     
MFN2 NM_014874.3 -?/. - c.119A>G r.(?) p.(Asn40Ser)


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