Variant #0000948099 (NC_000003.11:g.196199328_196199329del, NM_152617.3:c.1077_1078del (RNF168))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.196199328_196199329del |
DNA change (hg38) |
- |
Published as |
RNF168(NM_152617.3):c.1077_1078delAG (p.V361Dfs*10), RNF168(NM_152617.4):c.1077_1078del (p.(Val361Aspfs*10)) |
ISCN |
- |
DB-ID |
RNF168_000029 See all 2 reported entries |
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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-11-27 17:35:39 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|