Variant #0000974479 (NC_000002.11:g.174128561A>T, NM_016653.2:c.1640A>T (MAP3K20))

Chromosome 2
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.174128561A>T
DNA change (hg38) -
Published as MAP3K20(NM_016653.2):c.1640A>T (p.Q547L)
ISCN -
DB-ID MLK7-AS1_000004
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) 0.00114 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K20 NM_016653.2 -?/. - c.1640A>T r.(?) p.(Gln547Leu)
MLK7-AS1 NR_033882.1 -?/. - n.463+7678T>A r.(?) -


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