Variant #0000556602 (NC_000016.9:g.139764C>T, NM_001077350.2:c.1298G>A (NPRL3))

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.139764C>T
DNA change (hg38) g.89766C>T
Published as NPRL3(NM_001077350.2):c.1298G>A (p.R433Q), NPRL3(NM_001077350.3):c.1298G>A (p.(Arg433Gln)), NPRL3(NM_001243249.2):c.1223G>A (p.R408Q)
ISCN -
DB-ID MPG_000005 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) 9.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPG NM_001015052.2 -?/. - c.*3988C>T r.(=) p.(=)
NPRL3 NM_001077350.2 -?/. - c.1298G>A r.(?) p.(Arg433Gln)


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