Variant #0000557014 (NC_000016.9:g.1823027G>A, NM_002513.2:c.-1492C>T (NME3))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1823027G>A
DNA change (hg38) g.1773026G>A
Published as MRPS34(NM_001300900.2):c.94C>T (p.Q32*), MRPS34(NM_023936.2):c.94C>T (p.(Gln32Ter))
ISCN -
DB-ID MRPS34_000002 See all 3 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) 0.00044 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +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.-1492C>T r.(?) p.(=)
MRPS34 NM_023936.1 +/. - c.94C>T r.(?) p.(Gln32Ter)
SPSB3 NM_080861.3 +/. - c.*4071C>T r.(=) p.(=)


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