Variant #0000659152 (NC_000023.10:g.152991286del, NM_000033.3:c.565del (ABCD1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.152991286del
DNA change (hg38) g.153725831del
Published as ABCD1(NM_000033.4):c.565delC (p.R189Gfs*9)
ISCN -
DB-ID BCAP31_000037
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.565del r.(?) p.(Arg189GlyfsTer9)
BCAP31 NM_001256447.1 +/. - c.-1542del r.(?) p.(=)


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