Genomic variant #0000047986

Individual ID 00025118
Chromosome 19
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.36340187G>C
DNA change (hg38) g.35849285G>C
Published as -
ISCN -
DB-ID NPHS1_000006 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.01599 View details
Owner Inst.Human Genetics - Heidelberg




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
NPHS1 NM_004646.3 ?/. 7 c.791C>G - r.(?) p.(Pro264Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000025121 DNA SEQ-NG Blood - - 4 Inst.Human Genetics - Heidelberg