Variant #0000548963 (NC_000012.11:g.64784211_64784212insTA, NM_001099676.2:c.135_136insAT (C12orf56))
| Chromosome |
12 |
| 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.64784211_64784212insTA |
| DNA change (hg38) |
g.64390431_64390432insTA |
| Published as |
C12orf56(NM_001170633.1):c.135_136insAT (p.E46Mfs*11) |
| ISCN |
- |
| DB-ID |
C12orf56_000002 |
| 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-02 16:54:14 +02:00 (CEST) |

Variant on transcripts
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