Variant #0000608334 (NC_000003.11:g.134267991C>A, NM_025180.3:c.1155C>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.134267991C>A
DNA change (hg38) g.134549149C>A
Published as CEP63(NM_001042383.1):c.1017C>A (p.(Asn339Lys)), CEP63(NM_025180.4):c.1155C>A (p.N385K)
ISCN -
DB-ID CEP63_000009 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) 0.00208 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 2019-12-04 14:54:23 +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.-63225G>T r.(?) p.(=)
CEP63 NM_025180.3 -?/. - c.1155C>A r.(?) p.(Asn385Lys)


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