Variant #0000678732 (NC_000009.11:g.95237057_95237068del, NC_000009.11(NM_001012267.1):c.564+94916_564+94927del (CENPP))

Chromosome 9
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.95237057_95237068del
DNA change (hg38) -
Published as ASPN(NM_017680.5):c.144_155delTGATGATGATGA (p.D49_D52del)
ISCN -
DB-ID ASPN_000020
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPP NM_001012267.1 -?/. - c.564+94916_564+94927del r.(=) p.(=)
ECM2 NM_001393.3 -?/. - c.*21561_*21572del r.(=) p.(=)
OMD NM_005014.2 -?/. - c.-50569_-50558del r.(?) p.(=)
OGN NM_014057.3 -?/. - c.-70334_-70323del r.(?) p.(=)
ASPN NM_017680.4 -?/. - c.144_152del r.(?) p.(Asp48_Asp50del)
NOL8 NM_017948.5 -?/. - c.-149497_-149486del r.(?) p.(=)
IPPK NM_022755.5 -?/. - c.*141078_*141089del r.(=) p.(=)


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