Variant #0000304461 (NC_000003.11:g.132437887T>C, NM_153240.4:c.621A>G (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.132437887T>C
DNA change (hg38) g.132719043T>C
Published as NPHP3(NM_153240.4):c.621A>G (p.V207=)
ISCN -
DB-ID NPHP3_000042
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) 3.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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.*42517T>C r.(=) p.(=)
ACAD11 NM_032169.4 -?/. - c.-59292A>G r.(?) p.(=)
NPHP3 NM_153240.4 -?/. - c.621A>G r.(?) p.(Val207=)
NPHP3-ACAD11 NR_037804.1 -?/. - n.725A>G r.(?) -


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