Variant #0000336869 (NC_000008.10:g.100133397A>G, NC_000008.10(NM_017890.3):c.938-8A>G (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.100133397A>G
DNA change (hg38) g.99121169A>G
Published as -
ISCN -
DB-ID VPS13B_000354
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +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.*757112T>C r.(=) p.(=)
VPS13B NM_017890.3 +?/. - c.938-8A>G r.(=) p.(=)
VPS13B NM_152564.4 +?/. - c.938-8A>G r.(=) p.(=)


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