Variant #0000518034 (NC_000003.11:g.134277136G>A, NM_025180.3:c.1620G>A (CEP63))

Chromosome 3
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.134277136G>A
DNA change (hg38) g.134558294G>A
Published as CEP63(NM_025180.4):c.1620G>A (p.R540=)
ISCN -
DB-ID ANAPC13_000007
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) 0.00086 View details
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 2020-06-15 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANAPC13 NM_015391.3 -?/. - c.-72370C>T r.(?) p.(=)
CEP63 NM_025180.3 -?/. - c.1620G>A r.(?) p.(Arg540=)


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