Variant #0000561995 (NC_000017.10:g.43343939C>T, NM_003954.3:c.2543G>A (MAP3K14))

Chromosome 17
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.43343939C>T
DNA change (hg38) g.45266572C>T
Published as MAP3K14(NM_003954.5):c.2543G>A (p.R848Q)
ISCN -
DB-ID MAP3K14_000007
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K14 NM_003954.3 ?/. - c.2543G>A r.(?) p.(Arg848Gln)
SPATA32 NM_152343.2 ?/. - c.-4556G>A r.(?) p.(=)
MAP3K14-AS1 NR_024434.1 ?/. - n.69-541C>T r.(?) -


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