Variant #0000324850 (NC_000016.9:g.69362947T>C, NM_032382.4:c.*162A>G (COG8))

Chromosome 16
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.69362947T>C
DNA change (hg38) g.69329044T>C
Published as PDF(NM_022341.1):c.710A>G (p.(Tyr237Cys))
ISCN -
DB-ID COG8_000001
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) 0.00025 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS4A NM_013245.2 -?/. - c.*4735T>C r.(=) p.(=)
NIP7 NM_016101.4 -?/. - c.-10786T>C r.(?) p.(=)
PDF NM_022341.1 -?/. - c.710A>G r.(?) p.(Tyr237Cys)
COG8 NM_032382.4 -?/. - c.*162A>G r.(=) p.(=)


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