Variant #0000659754 (NC_000002.11:g.20189774C>T, NM_001006657.1:c.3G>A (WDR35))

Chromosome 2
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.20189774C>T
DNA change (hg38) g.19990013C>T
Published as -
ISCN -
DB-ID WDR35_000054
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 17:47:00 +02:00 (CEST)
Date last edited 2020-11-28 17:33:09 +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 +?/+ 1 c.3G>A r.(?) p.(Met1_Ala30delinsMetfs*4)


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