Variant #0000441404 (NC_000017.10:g.39942822_39942823del, NC_000017.10(NM_002230.2):c.-9+19_-9+20del (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.39942822_39942823del
DNA change (hg38) g.41786570_41786571del
Published as -9+17_-9+18del2
ISCN -
DB-ID JUP_000036
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs67537421
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 2009-09-01 15:35:06 +02:00 (CEST)
Date last edited 2020-07-13 13:38:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
JUP NM_002230.2 -/- 1i c.-9+19_-9+20del r.(=) p.(=) -


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