Variant #0000002829 (NC_000004.11:g.128859936A>T, MFSD8(NM_152778.2):c.754+2T>A)

Individual ID 00002829
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.128859936A>T
Reference Siintola et al. 2007 Am J Hum Genet 81: 136-46;Lehesjoki pers comm, Dvorakova pers comm
DB-ID MFSD8_000010
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 ./. 8i c.754+2T>A r.spl? p.? VariO:0136 DNA substitution; VariO:0316 transversion -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002829 ? ? MFSD8 1 Y Yang