Variant #0000461218 (NC_000018.9:g.50450196T>C, NM_005215.3:c.817T>C (DCC))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50450196T>C |
| DNA change (hg38) |
g.52923826T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DCC_000032 See all 2 reported entries |
| Variant remarks |
CADD - 26.7, REVEL - 0.902, M-CAP - 0.624, MPC - 1.00 |
| Reference |
PubMed: Bierhals 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In silico |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Ashley Marsh |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-12-19 10:34:12 +01:00 (CET) |
| Date last edited |
2020-07-14 19:07:53 +02:00 (CEST) |

Variant on transcripts
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