Variant #0000969706 (NC_000019.9:g.36341311T>A, NM_004646.3:c.563A>T (NPHS1))

Chromosome 19
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.36341311T>A
DNA change (hg38) -
Published as NPHS1(NM_004646.3):c.563A>T (p.(Asn188Ile), p.N188I), NPHS1(NM_004646.4):c.563A>T (p.N188I)
ISCN -
DB-ID NPHS1_000166 See all 4 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) 0.00611 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPHS1 NM_004646.3 -?/. - c.563A>T r.(?) p.(Asn188Ile)
KIRREL2 NM_032123.5 -?/. - c.-6711T>A r.(?) p.(=)


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