Variant #0000002832 (NC_000004.11:g.128851955G>T, MFSD8(NM_152778.2):c.881C>A)

Individual ID 00002832
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.128851955G>T
Reference Aiello et al. 2009 Hum Mutat 30: E350-40;Kousi et al. 2009 Brain 132:810-9;Elleder, pers comm
DB-ID MFSD8_000013
Frequency -
Average frequency (gnomAD v.2.1.1) 0 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     
MFSD8 NM_152778.2 ./. 10 c.881C>A r.(?) p.(Thr294Lys) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002832 ? ? MFSD8 1 Y Yang