Variant #0000965531 (NC_000009.11:g.95236999C>A, NC_000009.11(NM_001012267.1):c.564+94858C>A (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.95236999C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ASPN_000021
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) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CENPP NM_001012267.1 ?/. - c.564+94858C>A r.(=) p.(=)
ECM2 NM_001393.3 ?/. - c.*21598G>T r.(=) p.(=)
OMD NM_005014.2 ?/. - c.-50532G>T r.(?) p.(=)
OGN NM_014057.3 ?/. - c.-70297G>T r.(?) p.(=)
ASPN NM_017680.4 ?/. - c.181G>T r.(?) p.(Glu61*)
NOL8 NM_017948.5 ?/. - c.-149460G>T r.(?) p.(=)
IPPK NM_022755.5 ?/. - c.*141115G>T r.(=) p.(=)


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