Variant #0000654176 (NC_000002.11:g.110947862T>C, NC_000002.11(NM_000272.3):c.144-10601A>G (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.110947862T>C
DNA change (hg38) g.110190285T>C
Published as NPHP1(NM_000272.3):c.144-10601A>G
ISCN -
DB-ID NPHP1_000073
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +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.144-10601A>G r.(=) p.(=)
NPHP1 NM_001128178.1 -/. - c.144-10601A>G r.(=) p.(=)


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