Variant #0001020343 (NC_000014.8:g.65544706T>C, NM_002382.4:c.220A>G (MAX))
Chromosome |
14 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.65544706T>C |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
CHURC1-FNTB_000001 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Richarda de Voer |
Database submission license |
No license selected |
Created by |
Richarda de Voer |
Date created |
2025-01-10 19:19:09 +01:00 (CET) |
Date last edited |
2025-01-13 16:42:41 +01:00 (CET) |

Variant on transcripts
|