Variant #0000894286 (NC_000017.10:g.73839155C>T, NC_000017.10(NM_199242.2):c.262-1G>A (UNC13D))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73839155C>T
DNA change (hg38) -
Published as UNC13D(NM_199242.2):c.262-1G>A
ISCN -
DB-ID UNC13D_000034 See all 4 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.*3660G>A r.(=) p.(=)
UNC13D NM_199242.2 +/. - c.262-1G>A r.spl? p.?


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