Screening #0000017889

Individual ID 00017906
Template DNA
Technique DGGE;SEQ;SEQ-NG-I
Tissue -
Remarks -
Variants found? 2
Owner name Elisabet Ars Criach


Genes screened


AscendingSymbol     

Gene     

Chr     

Band

Transcripts     

Variants     

Unique variants     

Last updated     

Associated with diseases
NPHS1 nephrosis 1, congenital, Finnish type (nephrin) 19 q12-q13.1 1 317 192 2019-07-05 NPHS, NPHS-1



Variants found

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Chr     

Allele     

Effect     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     

Gene     

Codon change     

IDbase Accession Number     

VariO/DNA     

VariO/Protein     

VariO/RNA     

Exon     

DNA change (cDNA)     

Haplotype     

ClassClinical     

RNA change     

Protein     

P-domain     

Exon_old     

DNA/Legacy     

Function/GVS     

Predict/AGVGD     

Predict/Grantham     

Predict/MutationTaster     

Predict/PolyPhen     

Predict/PolyPhenScore     

Predict/SIFT     

Predicted     

Type/DNA     

Conservation     

CpG     

Enzyme activity     

mRNA level     

Predict/CADD     

Predict/Splice     

Protein level     
19 Maternal (confirmed) +/+ g.36321958G>A g.35831056G>A - - NPHS1_000117 - PubMed: Bullich 2015, Journal: Bullich 2015 - - Germline - - - 0 - Elisabet Ars Criach NPHS1 - - - - - 27 NM_004646.3:c.3478C>T - - r.(?) p.(Arg1160*) - - - - - - - - - - - - - - - - - - -
19 Paternal (confirmed) +/+ g.36341921G>C g.35851019G>C - - NPHS1_000023 - PubMed: Bullich 2015, Journal: Bullich 2015 - - Germline - - - 0 - Elisabet Ars Criach NPHS1 - - - - - 04 NM_004646.3:c.468C>G - - r.(?) p.(Tyr156*) - - - - - - - - - - - - - - - - - - -
Legend