Variant #0000697180 (NC_000017.10:g.58227435C>T, NM_000717.3:c.40C>T (CA4))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.58227435C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CA4_000013 See all 4 reported entries
Variant remarks expression cloning COS-7 cells shows protein retained in endoplasmatic reticulum, partially reduced protein processing and S and G2/M cell-cycle block; effects not seen in HEK293 cells
Reference PubMed: Pandor 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00025 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-10-07 14:15:31 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA4 NM_000717.3 +?/. - c.40C>T - p.Arg14Trp


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