Variant #0000864344 (NC_000016.9:g.169117A>C, NC_000016.9(NM_001077350.2):c.318+8T>G (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.169117A>C
DNA change (hg38) -
Published as NPRL3(NM_001077350.2):c.318+8T>G (p.(=))
ISCN -
DB-ID MPG_000015 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) 0.00033 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPG NM_001015052.2 -?/. - c.*33341A>C r.(=) p.(=)
NPRL3 NM_001077350.2 -?/. - c.318+8T>G r.(=) p.(=)


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