Variant #0000606052 (NC_000002.11:g.110936052T>A, NM_000272.3:c.277A>T (NPHP1))

Chromosome 2
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.110936052T>A
DNA change (hg38) g.110178475T>A
Published as NPHP1(NM_000272.3):c.277A>T (p.(Thr93Ser))
ISCN -
DB-ID NPHP1_000067
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +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.277A>T r.(?) p.(Thr93Ser)
NPHP1 NM_001128178.1 -?/. - c.277A>T r.(?) p.(Thr93Ser)


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