Variant #0000721641 (NC_000008.10:g.100147283G>A, NM_017890.3:c.1343G>A (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.100147283G>A
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.1343G>A (p.G448E)
ISCN -
DB-ID COX6C_000129
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) 3.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 ?/. - c.*743226C>T r.(=) p.(=)
VPS13B NM_017890.3 ?/. - c.1343G>A r.(?) p.(Gly448Glu)
VPS13B NM_152564.4 ?/. - c.1343G>A r.(?) p.(Gly448Glu)


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