Variant #0000979295 (NC_000011.9:g.108017985_108017988del, NC_000011.9(NM_000019.3):c.1164-12_1164-9del (ACAT1))
Chromosome |
11 |
Allele |
Unknown |
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.108017985_108017988del |
DNA change (hg38) |
- |
Published as |
ACAT1(NM_001386677.1):c.1173_1176del (p.(Phe391LeufsTer14)) |
ISCN |
- |
DB-ID |
ACAT1_000012 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|