Variant #0000675917 (NC_000001.10:g.6531575G>C, NM_020631.4:c.1254C>G (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.6531575G>C
DNA change (hg38) -
Published as PLEKHG5(NM_198681.3):c.1485C>G (p.P495=), PLEKHG5(NM_198681.4):c.1254C>G (p.P418=)
ISCN -
DB-ID PLEKHG5_000022 See all 2 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) 0.00451 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.1254C>G r.(?) p.(Pro418=)
ESPN NM_031475.2 -?/. - c.*11369G>C r.(=) p.(=)
TNFRSF25 NM_148965.1 -?/. - c.-5408C>G r.(?) p.(=)


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