Variant #0000266354 (NC_000019.9:g.30193721G>A, NM_001256047.1:c.324C>T (C19orf12))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.30193721G>A |
| DNA change (hg38) |
g.29702814G>A |
| Published as |
C19orf12(NM_001031726.3):c.357C>T (p.T119=), C19orf12(NM_001282931.3):c.132C>T (p.T44=), C19orf12(NM_031448.6):c.324C>T (p.T108=) |
| ISCN |
- |
| DB-ID |
C19orf12_000005 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) |
0.65598 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|