Variant #0000324430 (NC_000016.9:g.1822949C>A, NM_002513.2:c.-1414G>T (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.1822949C>A
DNA change (hg38) g.1772948C>A
Published as MRPS34(NM_023936.1):c.172G>T (p.(Val58Leu))
ISCN -
DB-ID MRPS34_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.-1414G>T r.(?) p.(=)
MRPS34 NM_023936.1 ?/. - c.172G>T r.(?) p.(Val58Leu)
SPSB3 NM_080861.3 ?/. - c.*4149G>T r.(=) p.(=)


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