Variant #0000718763 (NC_000002.11:g.38298421_38298433del, NM_000104.3:c.1064_1076del (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.38298421_38298433del
DNA change (hg38) -
Published as CYP1B1(NM_000104.3):c.1064_1076delGAGTGCAGGCAGA (p.R355Hfs*69), CYP1B1(NM_000104.4):c.1064_1076del (p.(Arg355Hisfs*69))
ISCN -
DB-ID CYP1B1_000017 See all 12 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) 0.00023 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP1B1 NM_000104.3 +/. - c.1064_1076del r.(?) p.(Arg355HisfsTer69) -
FAM82A1 NM_144713.3 +/. - c.*4288_*4300del r.(=) p.(=) -


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