Variant #0000786052 (NC_000003.11:g.120394885G>C, NC_000003.11(NM_000187.3):c.16-175C>G (HGD))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.120394885G>C |
| DNA change (hg38) |
g.120676038G>C |
| Published as |
ivs1-175C>G |
| ISCN |
- |
| DB-ID |
HGD_000126 |
| Variant remarks |
- |
| Reference |
Vilboux (2009) - data and classification copied from HGD mutations database |
| ClinVar ID |
- |
| dbSNP ID |
rs17140398 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2021-05-21 10:09:09 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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