Variant #0000688230 (NC_000001.10:g.6528320C>T, NM_020631.4:c.2576G>A (PLEKHG5))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6528320C>T
DNA change (hg38) -
Published as PLEKHG5(NM_198681.4):c.2576G>A (p.R859H)
ISCN -
DB-ID ESPN_000064
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) 0.00609 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG5 NM_020631.4 -/. - c.2576G>A r.(?) p.(Arg859His)
ESPN NM_031475.2 -/. - c.*8114C>T r.(=) p.(=)
TNFRSF25 NM_148965.1 -/. - c.-2153G>A r.(?) p.(=)


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