Variant #0000004748 (NC_000001.10:g.202568476G>A, SYT2(NM_177402.4):c.923C>T)

Individual ID 00004748
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.202568476G>A
Reference Herrmann DN1, Horvath R2, Sowden JE1, Gonzalez M, Sanchez-Mejias A3, Guan Z4, Whittaker RG5, Almodovar JL6, Lane M2, Bansagi B2, Pyle A2, Boczonadi V2, Lochmüller H(2014)
DB-ID SYT2_000002
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     
SYT2 NM_177402.4 ./. 8 c.923C>T r.(?) p.(Pro308Leu) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004748 ? ? SYT2 1 Y Yang