Variant #0000961132 (NC_000001.10:g.6532644C>T, NM_020631.4:c.1023G>A (PLEKHG5))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6532644C>T
DNA change (hg38) -
Published as PLEKHG5(NM_001265593.1):c.1230G>A (p.V410=)
ISCN -
DB-ID PLEKHG5_000092
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) 9.0E-5 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 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.1023G>A r.(?) p.(=)
TNFRSF25 NM_148965.1 -?/. - c.-6477G>A r.(?) p.(=)


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