Variant #0000000109 (NC_000023.11:g.139537049G>A, NM_000133.3:c.128G>A (F9))

Individual ID 00000016
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.139537049G>A
Published as -
Reference Balraj P et al. (2012), dbSNP, ClinVar
DB-ID F9_000004 See all 2 reported entries
dbSNP ID rs1275708479
Frequency -
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 2017-11-22 10:19:02 +08:00 (CST)
Date last edited 2021-09-13 12:23:55 +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.128G>A - r.(?) p.(Arg43Gln) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000023 DNA SEQ - 1 MyHVP