Variant #0001078569 (NC_000016.9:g.1756561A>G, NM_001318852.2:c.221A>G (MAPK8IP3))

Chromosome 16
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.1756561A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr16_007655
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1398696562
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 2026-06-24 12:03:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPK8IP3 NM_001318852.2 ?/. - c.221A>G r.(?) p.(Gln74Arg)


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