Variant #0000678243 (NC_000008.10:g.100871568del, NM_017890.3:c.10979del (VPS13B))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100871568del
DNA change (hg38) -
Published as VPS13B(NM_017890.4):c.10979del (p.(Pro3660LeufsTer5)), VPS13B(NM_017890.5):c.10979delC (p.P3660Lfs*5)
ISCN -
DB-ID COX6C_000118 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.*18943del r.(?) p.(=)
VPS13B NM_017890.3 +?/. - c.10979del r.(?) p.(Pro3660LeufsTer5)
VPS13B NM_152564.4 +?/. - c.10904del r.(?) p.(Pro3635LeufsTer5)


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