Variant #0000722596 (NC_000009.11:g.95077169A>G, NM_001012267.1:c.-11112A>G (CENPP))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95077169A>G
DNA change (hg38) -
Published as NOL8(NM_001256394.1):c.1534T>C (p.Y512H)
ISCN -
DB-ID CENPP_000003
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 2021-02-08 18:36:18 +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.-11112A>G r.(?) p.(=)
NOL8 NM_017948.5 -?/. - c.1738T>C r.(?) p.(Tyr580His)


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