Variant #0000867162 (NC_000023.10:g.152990979C>T, NM_000033.3:c.258C>T (ABCD1))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152990979C>T |
DNA change (hg38) |
- |
Published as |
ABCD1(NM_000033.3):c.258C>T (p.V86=, p.(Val86=)) |
ISCN |
- |
DB-ID |
ABCD1_000135 See all 2 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) |
0.00086 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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