Variant #0001042608 (NC_000019.9:g.1226494C>T, NM_000455.4:c.1150C>T (STK11))

Chromosome 19
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.1226494C>T
DNA change (hg38) -
Published as STK11(NM_000455.5):c.1150C>T (p.R384W)
ISCN -
DB-ID STK11_000737 See all 2 reported entries
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK11 NM_000455.4 ?/. - c.1150C>T r.(?) p.(Arg384Trp)
C19orf26 NM_152769.2 ?/. - c.*4398G>A r.(=) p.(=)


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