Variant #0000001852 (NC_000001.10:g.12069698C>T, MFN2(NM_014874.3):c.2119C>T)

Individual ID 00001852
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.12069698C>T
Reference Nicholson GA1, Magdelaine C, Zhu D, Grew S, Ryan MM, Sturtz F, Vallat JM, Ouvrier RA.(2008)
DB-ID MFN2_000002 See all 2 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00025 View details
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
MFN2 NM_014874.3 ./. 18 c.2119C>T r.(?) p.(Arg707Trp) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001852 ? ? MFN2 1 Y Yang