Variant #0000725503 (NC_000016.9:g.1816964G>C, NM_002513.2:c.*3686C>G (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.1816964G>C
DNA change (hg38) -
Published as MAPK8IP3(NM_001318852.1):c.3080G>C (p.R1027P)
ISCN -
DB-ID MRPS34_000016
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NME3 NM_002513.2 ?/. - c.*3686C>G r.(=) p.(=)
MRPS34 NM_023936.1 ?/. - c.*5258C>G r.(=) p.(=)


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