Variant #0000441394 (NC_000017.10:g.39925733G>A, NM_002230.2:c.405C>T (JUP))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39925733G>A
DNA change (hg38) g.41769481G>A
Published as -
ISCN -
DB-ID JUP_000006 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs17850807
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00798 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-01-30 10:50:26 +01:00 (CET)
Date last edited 2018-12-24 14:07:45 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
JUP NM_002230.2 -/- 3 c.405C>T r.(?) p.(=) Armadillo 1


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