Variant #0000965532 (NC_000009.11:g.95237024_95237026del, NC_000009.11(NM_001012267.1):c.564+94883_564+94885del (CENPP))

Chromosome 9
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.95237024_95237026del
DNA change (hg38) -
Published as ASPN(NM_017680.5):c.153_155delTGA (p.E51del)
ISCN -
DB-ID ASPN_000022
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPP NM_001012267.1 -/. - c.564+94883_564+94885del r.(=) p.(=)
ECM2 NM_001393.3 -/. - c.*21573_*21575del r.(=) p.(=)
OMD NM_005014.2 -/. - c.-50557_-50555del r.(?) p.(=)
OGN NM_014057.3 -/. - c.-70322_-70320del r.(?) p.(=)
ASPN NM_017680.4 -/. - c.156_158del r.(?) p.(Glu52del)
NOL8 NM_017948.5 -/. - c.-149485_-149483del r.(?) p.(=)
IPPK NM_022755.5 -/. - c.*141090_*141092del r.(=) p.(=)


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