Variant #0000502837 (NC_000001.10:g.12378223C>T, NM_015378.2:c.7243C>T (VPS13D))

Chromosome 1
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.12378223C>T
DNA change (hg38) g.12318166C>T
Published as VPS13D(NM_015378.2):c.7243C>T (p.(His2415Tyr)), VPS13D(NM_015378.4):c.7243C>T (p.H2415Y)
ISCN -
DB-ID VPS13D_000037 See all 2 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) 0.00173 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS13D NM_015378.2 -?/. - c.7243C>T r.(?) p.(His2415Tyr)


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