Variant #0000676626 (NC_000002.11:g.38302350C>T, NM_000104.3:c.182G>A (CYP1B1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38302350C>T
DNA change (hg38) -
Published as CYP1B1(NM_000104.3):c.181G>A (p.(Gly61Glu)), CYP1B1(NM_000104.3):c.182G>A (p.G61E, p.R61Q)
ISCN -
DB-ID CYP1B1_000012 See all 132 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) 0.00033 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 2020-08-06 14:59:34 +02:00 (CEST)
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     

Haplotype     
CYP1B1 NM_000104.3 ?/. - c.182G>A r.(?) p.(Gly61Glu) -


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