Variant #0000611359 (NC_000008.10:g.100887784C>G, NM_017890.3:c.11959C>G (VPS13B))

Chromosome 8
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.100887784C>G
DNA change (hg38) g.99875556C>G
Published as VPS13B(NM_017890.4):c.11959C>G (p.P3987A), VPS13B(NM_017890.5):c.11959C>G (p.P3987A), VPS13B(NM_152564.5):c.11884C>G (p.(Pro3962Ala))
ISCN -
DB-ID COX6C_000109 See all 4 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) 0.00083 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COX6C NM_004374.3 -?/. - c.*2725G>C r.(=) p.(=)
VPS13B NM_017890.3 -?/. - c.11959C>G r.(?) p.(Pro3987Ala)
VPS13B NM_152564.4 -?/. - c.11884C>G r.(?) p.(Pro3962Ala)


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