Variant #0000616559 (NC_000017.10:g.40817490C>A, NM_024927.4:c.*2655G>T (PLEKHH3))

Chromosome 17
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.40817490C>A
DNA change (hg38) g.42665472C>A
Published as TUBG2(NM_016437.2):c.607-4C>A (p.?)
ISCN -
DB-ID PLEKHH3_000005
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) 0.00226 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-13 14:04:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBG2 NM_016437.2 -?/. - c.607-4C>A r.spl? p.?
PLEKHH3 NM_024927.4 -?/. - c.*2655G>T r.(=) p.(=)


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