Variant #0000325417 (NC_000017.10:g.40828487_40828492dup, NM_024927.4:c.98_103dup (PLEKHH3))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40828487_40828492dup
DNA change (hg38) g.42676469_42676474dup
Published as PLEKHH3(NM_024927.4):c.103_104insGGGACG (p.?)
ISCN -
DB-ID PLEKHH3_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCR10 NM_016602.2 ?/. - c.*3087_*3092dup r.(=) p.(=)
PLEKHH3 NM_024927.4 ?/. - c.98_103dup r.(?) p.(Gly33_Asp34dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.