Variant #0000000846 (NC_000023.11:g.139530857G>C, NC_000023.11(NM_000133.3):c.88+5G>C (F9))

Individual ID 00000175
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.139530857G>C
Published as -
Reference Maimiza Zahari et al. (2018)
DB-ID F9_000008
dbSNP ID -
Frequency 1/11
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-22 16:16:41 +08:00 (CST)
Date last edited 2020-12-14 16:31:14 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
F9 NM_000133.3 +/. 1i c.88+5G>C - r.spl? p.? - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000190 DNA MLPA;PCRlr;SEQ F9 9 Nuur Athirah Binti Mohd Daud