Variant #0001042183 (NC_000017.10:g.73839322A>G, NM_199242.2:c.179T>C (UNC13D))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73839322A>G
DNA change (hg38) -
Published as UNC13D(NM_199242.3):c.179T>C (p.L60P)
ISCN -
DB-ID UNC13D_000113
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WBP2 NM_012478.3 +?/. - c.*3493T>C r.(=) p.(=)
UNC13D NM_199242.2 +?/. - c.179T>C r.(?) p.(Leu60Pro)


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