Variant #0000006596 (NC_000004.11:g.128861011A>G, MFSD8(NM_152778.2):c.695T>C)

Individual ID 00006602
Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.128861011A>G
Reference Ling Huang, et al. (2021)
DB-ID MFSD8_000031
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu
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 ?/. 7 c.695T>C r.(695u>c) p.(Leu232Pro) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000006626 ? ? MFSD8 1 XY Liu