Variant #0000001191 (NC_000002.11:g.179315184T>C, PRKRA(NM_001139517.1):c.-14A>G)
Individual ID |
00001191 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179315184T>C |
Reference |
Zech M1, Castrop F, Schormair B, Jochim A, Wieland T, Gross N, Lichtner P, Peters A, Gieger C, Meitinger T, Strom TM, Oexle K, Haslinger B, Winkelmann J.(2014) |
DB-ID |
PRKRA_000005 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-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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