Variant #0000508930 (NC_000002.11:g.110922080C>T, NC_000002.11(NM_000272.3):c.939+17G>A (NPHP1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.110922080C>T
DNA change (hg38) g.110164503C>T
Published as NPHP1(NM_000272.5):c.939+17G>A
ISCN -
DB-ID NPHP1_000057
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHP1 NM_000272.3 -/. - c.939+17G>A r.(=) p.(=)
NPHP1 NM_001128178.1 -/. - c.771+185G>A r.(=) p.(=)


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