Variant #0000508083 (NC_000001.10:g.6046264G>A, NM_015102.4:c.86C>T (NPHP4))

Chromosome 1
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.6046264G>A
DNA change (hg38) g.5986204G>A
Published as NPHP4(NM_015102.3):c.86C>T (p.(Thr29Met)), NPHP4(NM_015102.4):c.86C>T (p.T29M), NPHP4(NM_015102.5):c.86C>T (p.T29M)
ISCN -
DB-ID NPHP4_000098 See all 5 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) 0.02943 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     
NPHP4 NM_015102.4 -?/. - c.86C>T r.(?) p.(Thr29Met)


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