Variant #0000162759 (NC_000015.9:g.75014926T>G, NM_000499.3:c.513A>C (CYP1A1))

Chromosome 15
Allele Parent #1
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.75014926T>G
DNA change (hg38) g.74722585T>G
Published as 2216C>T
ISCN -
DB-ID CYP1A1_000004
Variant remarks -
Reference PubMed: SolusĀ 2004
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0007 View details
Owner Julia Lopez
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2017-01-30 15:15:56 +01:00 (CET)
Date last edited 2017-01-30 15:30:54 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP1A1 NM_000499.3 ?/. - c.513A>C r.(?) p.(=) -



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