Variant #0000002824 (NC_000004.11:g.128864984T>C, MFSD8(NM_152778.2):c.362A>G)

Individual ID 00002824
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.128864984T>C
Reference Stogmann et al. 2009. Neurogenet 10: 73-7
DB-ID MFSD8_000005
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
MFSD8 NM_152778.2 ./. 5 c.362A>G r.(?) p.(Tyr121Cys) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002824 ? ? MFSD8 1 Y Yang