Variant #0000329713 (NC_000003.11:g.180703710_180703713del, NM_005087.3:c.*9630_*9633del (FXR1))

Chromosome 3
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.180703710_180703713del
DNA change (hg38) g.180985922_180985925del
Published as DNAJC19(NM_001190233.1):c.205+4_205+7del (p.?)
ISCN -
DB-ID DNAJC19_000001
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 2020-06-16 09:11:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FXR1 NM_005087.3 ?/. - c.*9630_*9633del r.(=) p.(=)
DNAJC19 NM_145261.3 ?/. - c.280+4_280+7del r.spl? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.