Variant #0000001133 (NC_000023.11:g.139561821G>A, NM_000133.3:c.1136G>A (F9))

Individual ID 00000227
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.139561821G>A
Published as c.1136G/A
Reference dbSNP, (OMIM 0056), ClinVar
DB-ID F9_000017 See all 2 reported entries
dbSNP ID rs137852259
Frequency 3/10
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 2020-12-07 11:23:33 +08:00 (CST)
Date last edited 2021-08-23 16:02:32 +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 +/. 8 c.1136G>A c.1136G/A r.(?) p.(Arg379Gln) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000242 DNA PCR;SEQ F9 6 Nuur Athirah Binti Mohd Daud