Variant #0000001998 (NC_000006.11:g.18122506G>A, NHLRC1(NM_198586.2):c.332C>T)
Individual ID |
00001998 |
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18122506G>A |
Reference |
Chan EM1, Young EJ, Ianzano L, Munteanu I, Zhao X, Christopoulos CC, Avanzini G, Elia M, Ackerley CA, Jovic NJ, Bohlega S, Andermann E, Rouleau GA, Delgado-Escueta AV, Minassian BA, Scherer SW.(2003) |
DB-ID |
NHLRC1_000008 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.40315 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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