Variant #0000850794 (NC_000005.9:g.138268643_138268645del, NC_000005.9(NM_001903.2):c.2433+242_2433+244del (CTNNA1))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.138268643_138268645del |
| DNA change (hg38) |
- |
| Published as |
CTNNA1(NM_001290307.2):c.2500_2502delACT (p.T834del) |
| ISCN |
- |
| DB-ID |
CTNNA1_000053 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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