Individual #00000016

Reference Balraj P et al. (2012)
Gender -
Geographic origin -
Ethnic origin -
Population -
Remarks -
Microattribution -
Panel size 1
Diseases F9
Owner name MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 17:32:13 +08:00 (CST)
Date last edited N/A


Stop! No phenotypes found for this individual!



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000016 DNA SEQ F9 Not yet submitted MyHVP
0000000023 DNA SEQ - 1 MyHVP
0000000024 DNA SEQ F9 Not yet submitted MyHVP



Variants

1 entry on 1 page. Showing entry 1.
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Chr     

Allele     

Effect     

AscendingDNA change (genomic) (hg38)     

Published as     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Variant remarks     

Owner     

Gene     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
X Unknown ?/. g.139537049G>A - Balraj P et al. (2012), dbSNP, ClinVar F9_000004 rs1275708479 - - MyHVP F9 2 NM_000133.3:c.128G>A - r.(?) p.(Arg43Gln) - ClinVar
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