Variant #0000893546 (NC_000017.10:g.39927994_39927996dup, NM_002230.2:c.116_118dup (JUP))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39927994_39927996dup
DNA change (hg38) -
Published as JUP(NM_002230.2):c.116_118dupGCA (p.S39dup), JUP(NM_002230.4):c.116_118dupGCA (p.S39dup)
ISCN -
DB-ID JUP_000003 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
JUP NM_002230.2 +?/. - c.116_118dup r.(?) p.(Ser39dup) -


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