Variant #0000501863 (NC_000023.10:g.138612874T>G, F9(NM_000133.3):c.-50T>G)

Individual ID 00235454
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method EAHAD-CFDB
Clinical classification unclassified
DNA change (genomic) (Relative to hg19 / GRCh37) g.138612874T>G
DNA change (hg38) g.139530715T>G
Published as -
ISCN -
DB-ID F9_001107 See all 3 reported entries
Variant remarks -
Reference Unpublished
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Geoffrey Kemball-Cook
Database submission license Creative Commons Attribution-NonCommercial 4.0 InternationalCreative Commons License
Created by Daniel J Hampshire
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F9 NM_000133.3 ?/. _1 c.-50T>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000236558 ? ? - - F9 2 Geoffrey Kemball-Cook