Variant #0000680688 (NC_000016.9:g.87637921_87637935dup, NC_000016.9(NM_020655.2):c.382+787_382+801dup (JPH3))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.87637921_87637935dup
DNA change (hg38) -
Published as JPH3(NM_001271604.2):c.458_472dupCTGCTGCTGCTGCTG (p.A153_A157dup), JPH3(NM_001271604.4):c.458_472dup (p.(Ala153_Ala157dup))
ISCN -
DB-ID JPH3_000013 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
JPH3 NM_020655.2 ?/. - c.382+787_382+801dup - r.(=) p.(=)


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