Variant #0000926808 (NC_000019.9:g.1226669C>T, NC_000019.9(NM_000455.4):c.*16+7C>T (STK11))
| 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.1226669C>T |
| DNA change (hg38) |
- |
| Published as |
STK11(NM_000455.4):c.*16+7C>T (p.(=)), STK11(NM_000455.5):c.*16+7C>T |
| ISCN |
- |
| DB-ID |
C19orf26_000012 See all 2 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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