Variant #0000557018 (NC_000016.9:g.1825982C>T, NM_002513.2:c.-4447G>A (NME3))

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.1825982C>T
DNA change (hg38) g.1775981C>T
Published as EME2(NM_001257370.1):c.964C>T (p.(Gln322Ter))
ISCN -
DB-ID MRPS34_000013
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) 0.00822 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-4447G>A r.(?) p.(=)
MRPS34 NM_023936.1 -?/. - c.-2862G>A r.(?) p.(=)
SPSB3 NM_080861.3 -?/. - c.*1116G>A r.(=) p.(=)


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