Variant #0001032532 (NC_000002.11:g.174074554C>T, NM_016653.2:c.842C>T (MAP3K20))

Chromosome 2
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.174074554C>T
DNA change (hg38) -
Published as MAP3K20(NM_016653.3):c.842C>T (p.(Ala281Val))
ISCN -
DB-ID MLK7-AS1_000005
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) 0.00017 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 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     
MAP3K20 NM_016653.2 ?/. - c.842C>T r.(?) p.(Ala281Val)
MLK7-AS1 NR_033882.1 ?/. - n.1134G>A r.(?) -


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