Variant #0000508931 (NC_000002.11:g.110922279T>C, NM_000272.3:c.757A>G (NPHP1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.110922279T>C
DNA change (hg38) g.110164702T>C
Published as NPHP1(NM_000272.3):c.757A>G (p.K253E)
ISCN -
DB-ID NPHP1_000058
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) 7.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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.757A>G r.(?) p.(Lys253Glu)
NPHP1 NM_001128178.1 ?/. - c.757A>G r.(?) p.(Lys253Glu)


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