Variant #0000000099 (NC_000023.11:g.139567145C>T, NM_000133.3:c.*5074C>T (F9))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.139567145C>T
Published as -
Reference Balraj P et al. (2012)
DB-ID F9_000002
dbSNP ID -
Frequency 16
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 17:43:23 +08:00 (CST)
Date last edited 2017-11-22 09:42:14 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
F9 NM_000133.3 ./. 2 c.*5074C>T - r.(=) p.(=) - -