Variant #0000920661 (NC_000016.9:g.180520C>A, NC_000016.9(NM_001077350.2):c.188+1G>T (NPRL3))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.180520C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NPRL3_000010
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-03-05 17:14:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPRL3 NM_001077350.2 +?/. - c.188+1G>T r.(?) p.(?)


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