Variant #0000980509 (NC_000012.11:g.94761633T>C, NM_016122.2:c.1280A>G (CEP83))

Chromosome 12
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.94761633T>C
DNA change (hg38) -
Published as CEP83(NM_016122.3):c.1280A>G (p.(Glu427Gly))
ISCN -
DB-ID PLXNC1_000028
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLXNC1 NM_005761.2 ?/. - c.*62572T>C r.(=) p.(=)
CEP83 NM_016122.2 ?/. - c.1280A>G r.(?) p.(Glu427Gly)


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