Variant #0001050594 (NC_000002.11:g.38301998del, NM_000104.3:c.535del (CYP1B1))

Chromosome 2
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.38301998del
DNA change (hg38) -
Published as CYP1B1(NM_000104.3):c.535delG (p.A179Rfs*18), CYP1B1(NM_000104.4):c.535del (p.(Ala179Argfs*18))
ISCN -
DB-ID CYP1B1_001031 See all 4 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP1B1 NM_000104.3 +/. - c.535del r.(?) p.(Ala179Argfs*18) -


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