Variant #0000891865 (NC_000014.8:g.74756738G>A, NM_005050.3:c.1411C>T (ABCD4))
Chromosome |
14 |
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.74756738G>A |
DNA change (hg38) |
- |
Published as |
ABCD4(NM_005050.4):c.1411C>T (p.(Arg471Trp), p.R471W), ABCD4(NM_020325.2):c.1411C>T (p.R471W) |
ISCN |
- |
DB-ID |
ABCD4_000026 See all 4 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) |
0.00154 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|