Variant #0000951817 (NC_000019.9:g.4110540A>T, NM_030662.3:c.417T>A (MAP2K2))

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.4110540A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAP2K2_000047
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1165668205
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-27 21:10:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K2 NM_030662.3 ?/. - c.417T>A r.(?) p.(Ser139Arg)


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