Variant #0000517979 (NC_000003.11:g.132427031G>A, NM_153240.4:c.1189C>T (NPHP3))

Chromosome 3
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.132427031G>A
DNA change (hg38) g.132708187G>A
Published as NPHP3(NM_153240.4):c.1189C>T (p.R397C, p.(Arg397Cys)), NPHP3(NM_153240.5):c.1189C>T (p.R397C)
ISCN -
DB-ID ACAD11_000024 See all 10 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) 0.00303 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBA5 NM_024818.3 -?/. - c.*31661G>A r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-48436C>T r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.1189C>T r.(?) p.(Arg397Cys)
NPHP3-ACAD11 NR_037804.1 -?/. - n.1293C>T r.(?) -


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