Variant #0000559790 (NC_000016.9:g.89220556C>T, NM_174917.3:c.1672C>T (ACSF3))
Chromosome |
16 |
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.89220556C>T |
DNA change (hg38) |
g.89154148C>T |
Published as |
ACSF3(NM_001243279.2):c.1672C>T (p.R558W), ACSF3(NM_001243279.3):c.1672C>T (p.R558W), ACSF3(NM_174917.3):c.1672C>T (p.(Arg558Trp)), ACSF3(NM_17491...) |
ISCN |
- |
DB-ID |
ACSF3_000033 See all 5 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) |
0.00263 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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