Variant #0000001192 (NC_000007.13:g.94259041G>T, SGCE(NM_001099401.1):c.222C>A)

Individual ID 00001192
Chromosome 7
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94259041G>T
Reference Bonello M1, Larner AJ2, Alusi SH1.(2014)
DB-ID SGCE_000014
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SGCE NM_001099401.1 ./. 2 c.222C>A r.(?) p.(Tyr74*) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0015 protein truncation



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001192 ? ? SGCE 1 Y Yang