Variant #0000324853 (NC_000016.9:g.69368426T>G, NM_032382.4:c.1411A>C (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.69368426T>G
DNA change (hg38) g.69334523T>G
Published as COG8(NM_032382.4):c.1411A>C (p.(Lys471Gln))
ISCN -
DB-ID COG8_000005
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.-5307T>G r.(?) p.(=)
PDF NM_022341.1 ?/. - c.-3953A>C r.(?) p.(=)
COG8 NM_032382.4 ?/. - c.1411A>C r.(?) p.(Lys471Gln)


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