Variant #0000914496 (NC_000016.9:g.1815106C>T, NM_001318852.2:c.2373C>T (MAPK8IP3))

Chromosome 16
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.1815106C>T
DNA change (hg38) -
Published as MAPK8IP3(NM_001040439.2):c.2352C>T (p.A784=)
ISCN -
DB-ID MAPK8IP3_000022
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPK8IP3 NM_001318852.2 -?/. - c.2373C>T r.(?) p.(Ala791=)


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