Variant #0000001134 (NC_000023.11:g.139562070A>G, NM_000133.3:c.1385A>G (F9))

Individual ID 00000227
Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.139562070A>G
Published as c. 1385A/G
Reference dbSNP, ClinVar
DB-ID F9_000018
dbSNP ID rs561793582
Frequency 1/10
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 11:34:40 +08:00 (CST)
Date last edited 2021-08-23 16:03:29 +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.1385A>G c. 1385A/G r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

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