Variant #0000332680 (NC_000009.11:g.95285117A>G, NC_000009.11(NM_001012267.1):c.565-88479A>G (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.95285117A>G
DNA change (hg38) g.92522835A>G
Published as ECM2(NM_001197295.1):c.32T>C (p.(Leu11Pro))
ISCN -
DB-ID CENPP_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 2020-03-23 16:13:27 +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.565-88479A>G r.(=) p.(=)
ECM2 NM_001393.3 ?/. - c.32T>C r.(?) p.(Leu11Pro)
OMD NM_005014.2 ?/. - c.-98650T>C r.(?) p.(=)
OGN NM_014057.3 ?/. - c.-118415T>C r.(?) p.(=)
ASPN NM_017680.4 ?/. - c.-40573T>C r.(?) p.(=)
NOL8 NM_017948.5 ?/. - c.-197578T>C r.(?) p.(=)
IPPK NM_022755.5 ?/. - c.*92997T>C r.(=) p.(=)


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