Variant #0000000953 (NC_000003.12:g.15635477_15635483delinsTCC, NM_000060.4:c.98_104delinsTCC (BTD))
Individual ID |
00000194 |
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.15635477_15635483delinsTCC |
Published as |
- |
Reference |
M Mardhiah et al. (2019), ClinVar |
DB-ID |
BTD_000001 |
dbSNP ID |
- |
Frequency |
2/6 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-11-26 15:51:57 +08:00 (CST) |
Date last edited |
2020-12-14 17:04:16 +08:00 (CST) |

Variant on transcripts
Screenings
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