Variant #0000000931 (NC_000006.12:g.152462787G>A, NM_182961.3:c.2201C>T (SYNE1))

Individual ID 00000188
Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.152462787G>A
Published as P734L
Reference Shafina-Nadiawati Abdul et al. (2017)
DB-ID SYNE1_000004
dbSNP ID rs368462762
Frequency 1/9
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-25 14:46:19 +08:00 (CST)
Date last edited 2021-09-08 15:24:02 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
SYNE1 NM_182961.3 +/. 20 c.2201C>T - r.(?) p.(Pro734Leu) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000203 DNA PCR;SEQ;Western SYNE1 9 Nuur Athirah Binti Mohd Daud