Variant #0000518031 (NC_000003.11:g.134264664A>G, NC_000003.11(NM_025180.3):c.789+3A>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.134264664A>G
DNA change (hg38) g.134545822A>G
Published as CEP63(NM_001042383.1):c.789+3A>G (p.?), CEP63(NM_025180.4):c.789+3A>G
ISCN -
DB-ID CEP63_000005 See all 2 reported entries
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-15 15:50:13 +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.-59898T>C r.(?) p.(=)
CEP63 NM_025180.3 -?/. - c.789+3A>G r.spl? p.?


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