Variant #0001066936 (NC_000018.9:g.11880998C>T, NM_001142339.2:c.1010C>T (GNAL))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11880998C>T
DNA change (hg38) -
Published as GNAL(NM_182978.4):c.1241C>T (p.(Thr414Met))
ISCN -
DB-ID chr18_002972
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAL NM_001142339.2 ?/. - c.1010C>T r.(?) p.(Thr337Met)
CHMP1B NM_020412.4 ?/. - c.*28888C>T r.(=) p.(=)
MPPE1 NM_023075.5 ?/. - c.*3446G>A r.(=) p.(=)


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