Variant #0000266883 (NC_000016.9:g.69373414T>C, NM_032382.4:c.42A>G (COG8))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.69373414T>C
DNA change (hg38) g.69339511T>C
Published as COG8(NM_032382.5):c.42A>G (p.T14=)
ISCN -
DB-ID COG8_000008
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) 0.28099 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 2018-01-15 20:58:59 +01:00 (CET)
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.-319T>C r.(?) p.(=)
PDF NM_022341.1 -/. - c.-8941A>G r.(?) p.(=)
COG8 NM_032382.4 -/. - c.42A>G r.(?) p.(Thr14=)
TMED6 NM_144676.3 -/. - c.*3896A>G r.(=) p.(=)


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