Variant #0000549537 (NC_000012.11:g.94761635A>T, NM_016122.2:c.1278T>A (CEP83))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94761635A>T
DNA change (hg38) g.94367859A>T
Published as -
ISCN -
DB-ID PLXNC1_000004
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-02 17:45:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLXNC1 NM_005761.2 +/. - c.*62574A>T r.(=) p.(=)
CEP83 NM_016122.2 +/. - c.1278T>A r.(?) p.(Tyr426Ter)


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