Variant #0000961058 (NC_000001.10:g.43830676G>A, NM_001255.2:c.*1876G>A (CDC20))

Chromosome 1
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.43830676G>A
DNA change (hg38) -
Published as ELOVL1(NM_001256399.2):c.241C>T (p.L81=)
ISCN -
DB-ID CDC20_000011
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
CDC20 NM_001255.2 -?/. - c.*1876G>A r.(=) p.(=)
ELOVL1 NM_022821.3 -?/. - c.241C>T r.(?) p.(=)


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