Variant #0000724307 (NC_000012.11:g.94763792T>C, NM_016122.2:c.954A>G (CEP83))

Chromosome 12
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.94763792T>C
DNA change (hg38) -
Published as CEP83(NM_016122.2):c.954A>G (p.S318=)
ISCN -
DB-ID PLXNC1_000019
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
PLXNC1 NM_005761.2 -?/. - c.*64731T>C r.(=) p.(=)
CEP83 NM_016122.2 -?/. - c.954A>G r.(?) p.(Ser318=)


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