Variant #0000005768 (NC_000004.11:g.90749321C>T, SNCA(NM_000345.3):c.136G>A)

Individual ID 00005782
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.90749321C>T
Reference Pimentel MM et al. (2015)
DB-ID SNCA_000001 See all 6 reported entries
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SNCA NM_000345.3 ./. 3 c.136G>A r.(?) p.(Glu46Lys) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000005798 ? ? SNCA 1 XY Liu