Variant #0000001919 (NC_000012.11:g.32751500C>T, FGD4(NM_139241.2):c.670C>T)

Individual ID 00001919
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.32751500C>T
Reference Stendel C1, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J(2007)
DB-ID FGD4_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
FGD4 NM_139241.2 ./. 5 c.670C>T r.(?) p.(Arg224*) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001919 ? ? FGD4 1 Y Yang