Variant #0000324961 (NC_000016.9:g.87637930_87637935del, NC_000016.9(NM_020655.2):c.382+796_382+801del (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.87637930_87637935del
DNA change (hg38) g.87604324_87604329del
Published as JPH3(NM_001271604.2):c.431_436del (p.(Ala147_Ala148del)), JPH3(NM_001271604.2):c.467_472delCTGCTG (p.A156_A157del)
ISCN -
DB-ID JPH3_000005 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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+796_382+801del - r.(=) p.(=)


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