Variant #0000557011 (NC_000016.9:g.1818311C>T, NM_002513.2:c.*2339G>A (NME3))

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.1818311C>T
DNA change (hg38) g.1768310C>T
Published as MAPK8IP3(NM_001040439.1):c.3653C>T (p.(Ser1218Phe))
ISCN -
DB-ID MRPS34_000007 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NME3 NM_002513.2 ?/. - c.*2339G>A r.(=) p.(=)
MRPS34 NM_023936.1 ?/. - c.*3911G>A r.(=) p.(=)


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