Variant #0000575245 (NC_000023.10:g.21627454A>G, NM_014927.3:c.2411A>G (CNKSR2))

Chromosome X
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.21627454A>G
DNA change (hg38) g.21609336A>G
Published as CNKSR2(NM_001168647.1):c.2321A>G (p.(His774Arg)), CNKSR2(NM_014927.4):c.2411A>G (p.H804R), CNKSR2(NM_014927.5):c.2411A>G (p.H804R)
ISCN -
DB-ID CNKSR2_000016 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) 0.00015 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNKSR2 NM_014927.3 -?/. - c.2411A>G r.(?) p.(His804Arg)


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