Variant #0000515778 (NC_000002.11:g.38298394C>T, NM_000104.3:c.1103G>A (CYP1B1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38298394C>T
DNA change (hg38) g.38071251C>T
Published as CYP1B1(NM_000104.3):c.1102G>A (p.(Arg368His)), CYP1B1(NM_000104.3):c.1103G>A (p.R368Q)
ISCN -
DB-ID CYP1B1_001010 See all 18 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) 0.00595 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +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 -?/. - c.1103G>A r.(?) p.(Arg368His) -
FAM82A1 NM_144713.3 -?/. - c.*4261C>T r.(=) p.(=) -


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