Variant #0000293933 (NC_000001.10:g.6532673G>A, NM_020631.4:c.994C>T (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.6532673G>A
DNA change (hg38) g.6472613G>A
Published as PLEKHG5(NM_198681.3):c.1225C>T (p.R409W), PLEKHG5(NM_198681.4):c.994C>T (p.R332W)
ISCN -
DB-ID PLEKHG5_000026 See all 3 reported entries
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) 0.00113 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG5 NM_020631.4 ?/. - c.994C>T r.(?) p.(Arg332Trp)
TNFRSF25 NM_148965.1 ?/. - c.-6506C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.