Variant #0000324856 (NC_000016.9:g.69374245dup, NM_032382.4:c.-787dup (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.69374245dup
DNA change (hg38) g.69340342dup
Published as NIP7(NM_001199434.1):c.282+6_282+7insG (p.(=))
ISCN -
DB-ID NIP7_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) 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIP7 NM_016101.4 ?/. - c.282+10dup r.(=) p.(=)
PDF NM_022341.1 ?/. - c.-9769dup r.(?) p.(=)
COG8 NM_032382.4 ?/. - c.-787dup r.(?) p.(=)
TMED6 NM_144676.3 ?/. - c.*3068dup r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.