Variant #0000508204 (NC_000001.10:g.6520139A>G, NM_020631.4:c.*7484T>C (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.6520139A>G
DNA change (hg38) g.6460079A>G
Published as -
ISCN -
DB-ID ESPN_000025
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
PLEKHG5 NM_020631.4 ?/. - c.*7484T>C r.(=) p.(=)
ESPN NM_031475.2 ?/. - c.2498A>G r.(?) p.(Asp833Gly)
TNFRSF25 NM_148965.1 ?/. - c.*1355T>C r.(=) p.(=)


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