Variant #0000538666 (NC_000009.11:g.95228790T>C, NC_000009.11(NM_001012267.1):c.564+86649T>C (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.95228790T>C
DNA change (hg38) g.92466508T>C
Published as ASPN(NM_017680.5):c.448A>G (p.K150E)
ISCN -
DB-ID ASPN_000012
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 2020-08-06 14:59:34 +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+86649T>C r.(=) p.(=)
ECM2 NM_001393.3 ?/. - c.*29807A>G r.(=) p.(=)
OMD NM_005014.2 ?/. - c.-42323A>G r.(?) p.(=)
OGN NM_014057.3 ?/. - c.-62088A>G r.(?) p.(=)
ASPN NM_017680.4 ?/. - c.448A>G r.(?) p.(Lys150Glu)
NOL8 NM_017948.5 ?/. - c.-141251A>G r.(?) p.(=)
IPPK NM_022755.5 ?/. - c.*149324A>G r.(=) p.(=)


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