Variant #0000681388 (NC_000019.9:g.36359644G>T, NM_004646.3:c.-16905C>A (NPHS1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.36359644G>T
DNA change (hg38) -
Published as APLP1(NM_001024807.2):c.106G>T (p.A36S)
ISCN -
DB-ID NPHS1_000209
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APLP1 NM_001024807.1 ?/. - c.106G>T r.(?) p.(Ala36Ser)
NPHS1 NM_004646.3 ?/. - c.-16905C>A r.(?) p.(=)
KIRREL2 NM_032123.5 ?/. - c.*2206G>T r.(=) p.(=)


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