Variant #0000336043 (NC_000023.10:g.152989463G>T, NM_000033.3:c.-1259G>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.152989463G>T
DNA change (hg38) g.153724008G>T
Published as BCAP31(NM_001139441.1):c.-45+8C>A (p.(=))
ISCN -
DB-ID BCAP31_000011
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) 0.01051 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +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.-1259G>T r.(?) p.(=)
BCAP31 NM_001256447.1 -?/. - c.-45+326C>A r.(=) p.(=)


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