Variant #0000962496 (NC_000003.11:g.134264578G>A, NM_025180.3:c.706G>A (CEP63))

Chromosome 3
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.134264578G>A
DNA change (hg38) -
Published as CEP63(NM_025180.3):c.706G>A (p.(Asp236Asn))
ISCN -
DB-ID ANAPC13_000020
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) 0.00011 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 2024-02-26 20:06:56 +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     
ANAPC13 NM_015391.3 ?/. - c.-59812C>T r.(?) p.(=)
CEP63 NM_025180.3 ?/. - c.706G>A r.(?) p.(Asp236Asn)


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