Variant #0000676832 (NC_000003.11:g.134280326A>G, NM_025180.3:c.2061A>G (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.134280326A>G
DNA change (hg38) -
Published as CEP63(NM_025180.4):c.2061A>G (p.E687=)
ISCN -
DB-ID ANAPC13_000015
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.-75560T>C r.(?) p.(=)
CEP63 NM_025180.3 -?/. - c.2061A>G r.(?) p.(Glu687=)


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