Variant #0000080752 (NC_000002.11:g.38298203G>C, NM_000104.3:c.1294C>G (CYP1B1))

Chromosome 2
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.38298203G>C
DNA change (hg38) g.38071060G>C
Published as -
ISCN -
DB-ID CYP1B1_000003 See all 47 reported entries
Variant remarks expression cloning yeast, normal expression/folding, normal clearance (estradiol)
Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message.
Reference PubMed: Aklillu 2002
ClinVar ID -
dbSNP ID rs1056836
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-05-20 12:49:57 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP1B1 NM_000104.3 -/. 3 c.1294C>G - p.Leu432Val -


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