Variant #0000563120 (NC_000017.10:g.73840320C>T, NM_199242.2:c.99G>A (UNC13D))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73840320C>T
DNA change (hg38) g.75844239C>T
Published as UNC13D(NM_199242.2):c.99G>A (p.P33=)
ISCN -
DB-ID UNC13D_000071
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) 0.00158 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-14 13:01:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WBP2 NM_012478.3 -?/. - c.*2495G>A r.(=) p.(=)
UNC13D NM_199242.2 -?/. - c.99G>A r.(?) p.(Pro33=)


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