Variant #0000300331 (NC_000002.11:g.110959026G>T, NM_000272.3:c.115C>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.110959026G>T
DNA change (hg38) g.110201449G>T
Published as NPHP1(NM_000272.3):c.115C>A (p.P39T), NPHP1(NM_000272.4):c.115C>A (p.P39T)
ISCN -
DB-ID NPHP1_000040 See all 4 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) 0.02713 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHP1 NM_000272.3 -/. - c.115C>A r.(?) p.(Pro39Thr)
NPHP1 NM_001128178.1 -/. - c.115C>A r.(?) p.(Pro39Thr)


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