Variant #0000575257 (NC_000023.10:g.21674897A>C, NM_014927.3:c.*4258A>C (CNKSR2))

Chromosome X
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.21674897A>C
DNA change (hg38) g.21656779A>C
Published as KLHL34(NM_153270.1):c.1010T>G (p.(Val337Gly))
ISCN -
DB-ID CNKSR2_000045
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNKSR2 NM_014927.3 ?/. - c.*4258A>C r.(=) p.(=)
KLHL34 NM_153270.1 ?/. - c.1010T>G r.(?) p.(Val337Gly)


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