Variant #0001024183 (NC_000001.10:g.47034174A>C, NC_000001.10(NM_003684.5):c.617-4T>G (MKNK1))

Chromosome 1
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.47034174A>C
DNA change (hg38) -
Published as MKNK1(NM_003684.7):c.581-4T>G
ISCN -
DB-ID KNCN_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KNCN NM_001097611.1 -?/. - c.-17287T>G r.(?) p.(=)
MKNK1 NM_003684.5 -?/. - c.617-4T>G r.spl? p.?
MKNK1-AS1 NR_038403.1 -?/. - n.692A>C r.(?) -


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