Variant #0000692344 (NC_000017.10:g.40828463_40828464insTCTCGT, NM_024927.4:c.119_120insCGAGAA (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.40828463_40828464insTCTCGT
DNA change (hg38) -
Published as PLEKHH3(NM_024927.4):c.119_120insCGAGAA (p.(AspGluLys40dup)), PLEKHH3(NM_024927.5):c.119_120insCGAGAA (p.E40delinsDEK)
ISCN -
DB-ID PLEKHH3_000002 See all 2 reported entries
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) 0.00036 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCR10 NM_016602.2 ?/. - c.*3108_*3109insCGAGAA r.(=) p.(=)
PLEKHH3 NM_024927.4 ?/. - c.119_120insCGAGAA r.(?) p.(Glu40delinsAspGluLys)


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