Variant #0000692027 (NC_000016.9:g.23716289C>T, NM_005030.3:c.*14905C>T (PLK1))

Chromosome 16
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.23716289C>T
DNA change (hg38) -
Published as ERN2(NM_001308220.1):c.769G>A (p.A257T)
ISCN -
DB-ID ERN2_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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
PLK1 NM_005030.3 -?/. - c.*14905C>T r.(=) p.(=)
ERN2 NM_033266.3 -?/. - c.769G>A r.(?) p.(Ala257Thr)


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