Variant #0000538672 (NC_000009.11:g.95237063_95237068dup, NC_000009.11(NM_001012267.1):c.564+94922_564+94927dup (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.95237063_95237068dup
DNA change (hg38) g.92474781_92474786dup
Published as ASPN(NM_017680.5):c.147_152dupTGATGA (p.D49_D50dup)
ISCN -
DB-ID ASPN_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPP NM_001012267.1 -/. - c.564+94922_564+94927dup r.(=) p.(=)
ECM2 NM_001393.3 -/. - c.*21567_*21572dup r.(=) p.(=)
OMD NM_005014.2 -/. - c.-50563_-50558dup r.(?) p.(=)
OGN NM_014057.3 -/. - c.-70328_-70323dup r.(?) p.(=)
ASPN NM_017680.4 -/. - c.144_152dup r.(?) p.(Asp48_Asp50dup)
NOL8 NM_017948.5 -/. - c.-149491_-149486dup r.(?) p.(=)
IPPK NM_022755.5 -/. - c.*141084_*141089dup r.(=) p.(=)


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