Variant #0001032533 (NC_000002.11:g.174085981G>A, NC_000002.11(NM_016653.2):c.987+4003G>A (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.174085981G>A
DNA change (hg38) -
Published as MAP3K20(NM_133646.3):c.1091G>A (p.(Ser364Asn))
ISCN -
DB-ID MLK7-AS1_000006
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) 0.00014 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.987+4003G>A r.(=) p.(=)
MLK7-AS1 NR_033882.1 -?/. - n.464-5417C>T r.(?) -


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