Variant #0000574321 (NC_000023.10:g.152991018C>T, NM_000033.3:c.297C>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.152991018C>T
DNA change (hg38) g.153725563C>T
Published as ABCD1(NM_000033.3):c.297C>T (p.A99=)
ISCN -
DB-ID BCAP31_000019
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCD1 NM_000033.3 -?/. - c.297C>T r.(?) p.(Ala99=)
BCAP31 NM_001256447.1 -?/. - c.-1274G>A r.(?) p.(=)


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