Variant #0000554755 (NC_000015.9:g.51514572G>A, NM_000103.3:c.602C>T (CYP19A1))

Chromosome 15
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.51514572G>A
DNA change (hg38) g.51222375G>A
Published as CYP19A1(NM_000103.3):c.602C>T (p.(Thr201Met)), CYP19A1(NM_031226.3):c.602C>T (p.T201M)
ISCN -
DB-ID CYP19A1_000006 See all 4 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) 0.02371 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP19A1 NM_000103.3 -/. - c.602C>T r.(?) p.(Thr201Met) -


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