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 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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