Variant #0000659755 (NC_000002.11:g.20135290T>A, NM_001006657.1:c.2522A>T (WDR35))

Chromosome 2
Allele Paternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.20135290T>A
DNA change (hg38) g.19935529T>A
Published as -
ISCN -
DB-ID WDR35_000001 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Joanna Walczak-Sztulpa
Database submission license No license selected
Created by Joanna Walczak-Sztulpa
Date created 2020-03-30 18:05:41 +02:00 (CEST)
Date last edited 2020-11-25 06:28:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR35 NM_001006657.1 +?/+? 22 c.2522A>T r.(?) p.(Asp841Val)


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