Variant #0000003813 (NC_000004.11:g.90749307A>T, SNCA(NM_000345.3):c.150T>A)

Individual ID 00003813
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.90749307A>T
Reference Khalaf O1, Fauvet B1, Oueslati A1, Dikiy I2, Mahul-Mellier AL1, Ruggeri FS3, Mbefo MK1, Vercruysse F1, Dietler G3, Lee SJ4, Eliezer D2, Lashuel HA5.(2014)
DB-ID SNCA_000006 See all 6 reported entries
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     
SNCA NM_000345.3 ./. 3 c.150T>A r.(?) p.(His50Gln) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000003813 ? ? SNCA 1 Y Yang