Variant #0000862479 (NC_000011.9:g.2189158G>T, NM_199292.2:c.675C>A (TH))
| Chromosome |
11 |
| 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.2189158G>T |
| DNA change (hg38) |
- |
| Published as |
TH(NM_199292.2):c.675C>A (p.F225L) |
| ISCN |
- |
| DB-ID |
TH_000071 |
| 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) |
0.00026 View details |
| 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 15:51:19 +02:00 (CEST) |
| Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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