Variant #0000566799 (NC_000019.9:g.30193732C>T, NM_001256047.1:c.313G>A (C19orf12))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.30193732C>T |
| DNA change (hg38) |
g.29702825C>T |
| Published as |
C19orf12(NM_001031726.3):c.346G>A (p.V116M), C19orf12(NM_001031726.4):c.313G>A (p.V105M), C19orf12(NM_001282931.1):c.121G>A (p.V41M) |
| ISCN |
- |
| DB-ID |
C19orf12_000006 See all 3 reported entries |
| 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) |
0.00096 View details |
| 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 |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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