Variant #0000304428 (NC_000002.11:g.110920625C>T, NM_000272.3:c.1027G>A (NPHP1))

Chromosome 2
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.110920625C>T
DNA change (hg38) g.110163048C>T
Published as NPHP1(NM_000272.3):c.1027G>A (p.G343R), NPHP1(NM_000272.4):c.1027G>A (p.G343R), NPHP1(NM_207181.4):c.1024G>A (p.G342R)
ISCN -
DB-ID NPHP1_000001 See all 15 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) 0.00012 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 2018-01-15 20:58:59 +01:00 (CET)
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.1027G>A r.(?) p.(Gly343Arg)
NPHP1 NM_001128178.1 +?/. - c.859G>A r.(?) p.(Gly287Arg)


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