Variant #0000818483 (NC_000012.11:g.28122956A>G, NC_000012.11(NM_198965.1):c.-23+2T>C (PTHLH))
| Chromosome |
12 |
| 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.28122956A>G |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PTHLH_000014 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs761025088 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2021-11-02 14:00:01 +01:00 (CET) |
| Date last edited |
2022-09-26 12:22:42 +02:00 (CEST) |

Variant on transcripts
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