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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCD1 NM_000033.3 -?/. - c.258C>T r.(?) p.(Val86=)
BCAP31 NM_001256447.1 -?/. - c.-1235G>A r.(?) p.(=)


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