Variant #0000698120 (NC_000019.9:g.36498133T>G, NM_001039876.1:c.317A>C (SYNE4))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36498133T>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SYNE4_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs200994810
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00061 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2020-10-19 11:37:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNE4 NM_001039876.1 -?/. - c.317A>C r.(?) p.(Gln106Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.