Variant #0000848920 (NC_000002.11:g.110922206C>T, NM_000272.3:c.830G>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.110922206C>T
DNA change (hg38) -
Published as NPHP1(NM_000272.3):c.830G>A (p.R277Q), NPHP1(NM_000272.4):c.830G>A (p.R277Q), NPHP1(NM_000272.5):c.830G>A (p.R277Q)
ISCN -
DB-ID NPHP1_000026 See all 3 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) 0.00043 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHP1 NM_000272.3 -/. - c.830G>A r.(?) p.(Arg277Gln)
NPHP1 NM_001128178.1 -/. - c.771+59G>A r.(=) p.(=)


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