Variant #0000332670 (NC_000009.11:g.95237066_95237068dup, NC_000009.11(NM_001012267.1):c.564+94925_564+94927dup (CENPP))

Chromosome 9
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.95237066_95237068dup
DNA change (hg38) g.92474784_92474786dup
Published as ASPN(NM_001193335.1):c.150_152dup (p.(Asp51dup))
ISCN -
DB-ID ASPN_000002
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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPP NM_001012267.1 ?/. - c.564+94925_564+94927dup r.(=) p.(=)
ECM2 NM_001393.3 ?/. - c.*21570_*21572dup r.(=) p.(=)
OMD NM_005014.2 ?/. - c.-50560_-50558dup r.(?) p.(=)
OGN NM_014057.3 ?/. - c.-70325_-70323dup r.(?) p.(=)
ASPN NM_017680.4 ?/. - c.147_152dup r.(?) p.(Asp49_Asp50dup)
NOL8 NM_017948.5 ?/. - c.-149488_-149486dup r.(?) p.(=)
IPPK NM_022755.5 ?/. - c.*141087_*141089dup r.(=) p.(=)


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