Variant #0000996811 (NC_000008.10:g.100115333T>C, NM_017890.3:c.565T>C (VPS13B))

Chromosome 8
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.100115333T>C
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.565T>C (p.F189L), VPS13B(NM_017890.5):c.565T>C (p.F189L)
ISCN -
DB-ID VPS13B_000180 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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +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     
COX6C NM_004374.3 ?/. - c.*775176A>G r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.565T>C r.(?) p.(Phe189Leu)
VPS13B NM_152564.4 ?/. - c.565T>C r.(?) p.(Phe189Leu)


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