Variant #0000961133 (NC_000001.10:g.6533112_6533118dup, NM_020631.4:c.912_918dup (PLEKHG5))

Chromosome 1
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.6533112_6533118dup
DNA change (hg38) -
Published as PLEKHG5(NM_001265593.1):c.1119_1125dupTGAAGAC (p.E376*)
ISCN -
DB-ID PLEKHG5_000056 See all 5 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) 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     
PLEKHG5 NM_020631.4 ?/. - c.912_918dup r.(?) p.(Glu307Ter)
TNFRSF25 NM_148965.1 ?/. - c.-6951_-6945dup r.(?) p.(=)


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