Variant #0000965743 (NC_000010.10:g.52569681_52569683del, NM_001198819.1:c.1642_1644del (A1CF))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52569681_52569683del |
DNA change (hg38) |
- |
Published as |
A1CF(NM_001198819.2):c.1642_1644delGCT (p.A548del) |
ISCN |
- |
DB-ID |
A1CF_000001 |
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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2024-02-26 20:06:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|