Variant #0000911117 (NC_000001.10:g.6533303C>T, NC_000001.10(NM_020631.4):c.795+8G>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.6533303C>T
DNA change (hg38) -
Published as PLEKHG5(NM_001265593.1):c.1002+8G>A
ISCN -
DB-ID PLEKHG5_000089
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) 0.00264 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 2023-01-11 15:44:22 +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.795+8G>A r.(=) p.(=)
TNFRSF25 NM_148965.1 -/. - c.-7136G>A r.(?) p.(=)


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