Variant #0000328998 (NC_000022.10:g.37964153C>T, NM_152243.2:c.502C>T (CDC42EP1))

Chromosome 22
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.37964153C>T
DNA change (hg38) g.37568146C>T
Published as CDC42EP1(NM_152243.2):c.502C>T (p.(Arg168Cys))
ISCN -
DB-ID CDC42EP1_000002
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LGALS2 NM_006498.2 ?/. - c.*2117G>A r.(=) p.(=)
CDC42EP1 NM_152243.2 ?/. - c.502C>T r.(?) p.(Arg168Cys)


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