Variant #0000888067 (NC_000007.13:g.99359655G>A, NC_000007.13(NM_017460.5):c.1253+9C>T (CYP3A4))

Chromosome 7
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.99359655G>A
DNA change (hg38) -
Published as CYP3A4(NM_017460.6):c.1253+9C>T
ISCN -
DB-ID CYP3A4_000068
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) 0.00123 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP3A4 NM_001202855.2 -?/. - c.1250+9C>T r.(=) p.(=) -
CYP3A4 NM_017460.5 -?/. - c.1253+9C>T r.(=) p.(=) -


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