Variant #0000081251 (NC_000010.10:g.?, NC_000010.10(NM_000771.3):c.168+83? (CYP2C9))

Chromosome 10
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.?
DNA change (hg38) -
Published as IVS1+83 g.-251A>C
ISCN -
DB-ID CYP2C9_001038 See all 68 reported entries
Variant remarks -
Reference PubMed: Goldestein 2009
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license No license selected
Created by Annemarie Schop (student)
Date created 2013-03-06 10:21:26 +01:00 (CET)
Date last edited 2013-03-08 00:03:02 +01:00 (CET)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2C9 NM_000771.3 -?/. 1i c.168+83? r.(?) p.(=) -



Screenings

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