Variant #0000952349 (NC_000017.10:g.61417478A>G, NM_025185.3:c.1370A>G (TANC2))
Individual ID |
00443879 |
Chromosome |
17 |
Allele |
Both (homozygous) |
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.61417478A>G |
DNA change (hg38) |
g.63340117A>G |
Published as |
NM_025185:c.1370A>G |
ISCN |
- |
DB-ID |
TANC2_000045 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: Chatron 2020 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-12-05 14:09:46 +01:00 (CET) |
Date last edited |
2025-03-11 19:58:31 +01:00 (CET) |

Variant on transcripts
Screenings
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