Variant #0000854603 (NC_000016.9:g.69368746C>T, NM_032382.4:c.1091G>A (COG8))

Chromosome 16
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.69368746C>T
DNA change (hg38) -
Published as COG8(NM_032382.5):c.1091G>A (p.R364Q)
ISCN -
DB-ID COG8_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIP7 NM_016101.4 ?/. - c.-4987C>T r.(?) p.(=)
PDF NM_022341.1 ?/. - c.-4273G>A r.(?) p.(=)
COG8 NM_032382.4 ?/. - c.1091G>A r.(?) p.(Arg364Gln)


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