Variant #0001060438 (NC_000002.11:g.174074549_174074551del, NM_016653.2:c.837_839del (MAP3K20))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.174074549_174074551del
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAP3K20_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2106303300
Origin Unknown
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 2025-12-02 13:59:01 +01:00 (CET)
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.837_839del r.(?) p.(Asn279del)


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