Variant #0000000910 (NC_000023.11:g.139537345_139537349delTCTTT, F9(NM_000133.3):c.253-17_253-13delTCTTT)

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.139537345_139537349delTCTTT
Published as -
Reference Maimiza Zahari et al. (2018)
DB-ID F9_000012
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
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 +/. 2i c.253-17_253-13delTCTTT - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

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