Variant #0000508222 (NC_000001.10:g.6533528G>A, NC_000001.10(NM_020631.4):c.592-14C>T (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.6533528G>A
DNA change (hg38) g.6473468G>A
Published as PLEKHG5(NM_198681.4):c.592-14C>T
ISCN -
DB-ID PLEKHG5_000041
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) 0.00108 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 2019-07-18 18:22:55 +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.592-14C>T r.(=) p.(=)
TNFRSF25 NM_148965.1 -/. - c.-7361C>T r.(?) p.(=)


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