Variant #0000441393 (NC_000017.10:g.39928011G>A, NM_002230.2:c.96C>T (JUP))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39928011G>A
DNA change (hg38) g.41771759G>A
Published as -
ISCN -
DB-ID JUP_000002
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs11655659
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-01-30 10:39:22 +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 -/? 2 c.96C>T r.(?) p.(=) N-terminus


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