Variant #0000977941 (NC_000007.13:g.99367392C>G, NM_017460.5:c.520G>C (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.99367392C>G
DNA change (hg38) -
Published as CYP3A4(NM_017460.6):c.520G>C (p.D174H)
ISCN -
DB-ID CYP3A4_000045 See all 3 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) 0.00193 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 2024-04-19 20:27:30 +02:00 (CEST)
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.520G>C r.(?) p.(Asp174His) -
CYP3A4 NM_017460.5 -?/. - c.520G>C r.(?) p.(Asp174His) -


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