Variant #0000571362 (NC_000022.10:g.19929268T>C, NM_000754.3:c.-244T>C (COMT))
| Chromosome |
22 |
| 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.19929268T>C |
| DNA change (hg38) |
g.19941745T>C |
| Published as |
TXNRD2(NM_001282512.2):c.59A>G (p.Q20R) |
| ISCN |
- |
| DB-ID |
ARVCF_000016 |
| 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 |
2020-07-17 10:49:43 +02:00 (CEST) |

Variant on transcripts
|