Variant #0000248513 (NC_000002.11:g.38298150A>G, NM_000104.3:c.1347T>C (CYP1B1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38298150A>G
DNA change (hg38) g.38071007A>G
Published as CYP1B1(NM_000104.4):c.1347T>C (p.D449=)
ISCN -
DB-ID CYP1B1_001002 See all 9 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) 0.63426 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.1347T>C r.(?) p.(Asp449=) -
FAM82A1 NM_144713.3 -/. - c.*4017A>G r.(=) p.(=) -


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