Variant #0000003195 (NC_000023.11:g.101360572T>C, NM_000061.2:c.772A>G (BTK))
Individual ID |
00000832 |
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.101360572T>C |
Published as |
g. 36712A>G |
Reference |
Intan Juliana Abd Hamid et al. (2020) |
DB-ID |
BTK_000008 |
dbSNP ID |
- |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Noorzalifah Binti Mazuki |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Noorzalifah Binti Mazuki |
Date created |
2021-08-10 12:29:24 +08:00 (CST) |
Date last edited |
2022-01-25 09:34:50 +08:00 (CST) |

Variant on transcripts
Screenings
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