Variant #0000926157 (NC_000016.9:g.180593G>C, NC_000016.9(NM_001077350.2):c.119-3C>G (NPRL3))

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.180593G>C
DNA change (hg38) -
Published as NPRL3(NM_001077350.3):c.119-3C>G, NPRL3(NM_001243249.2):c.119-3C>G
ISCN -
DB-ID MPG_000030 See all 2 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) 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPG NM_001015052.2 ?/. - c.*44817G>C r.(=) p.(=)
NPRL3 NM_001077350.2 ?/. - c.119-3C>G r.spl? p.?


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