Variant #0001050536 (NC_000002.11:g.20194084dup, NM_001006657.1:c.-4308dup (WDR35))

Chromosome 2
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.20194084dup
DNA change (hg38) -
Published as MATN3(NM_002381.5):c.1381dup (p.(Tyr461Leufs*8))
ISCN -
DB-ID MATN3_000057
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
WDR35 NM_001006657.1 ?/. - c.-4308dup r.(?) p.(=) -
MATN3 NM_002381.4 ?/. - c.1381dup r.(?) p.(Tyr461Leufs*8) -


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