Variant #0000016974 (NC_000018.9:g.11868544G>T, NM_001142339.2:c.682G>T (GNAL))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11868544G>T
DNA change (hg38) g.11868545G>T
Published as -
ISCN -
DB-ID GNAL_000001
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Satya Vemula
Database submission license No license selected
Created by Satya Vemula
Date created 2013-01-24 21:16:01 +01:00 (CET)
Date last edited 2013-01-24 22:14:13 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAL NM_001142339.2 ?/? 10 c.682G>T r.(?) p.(Val228Phe)


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