Variant #0000676889 (NC_000003.11:g.180702494T>G, NM_005087.3:c.*8414T>G (FXR1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.180702494T>G
DNA change (hg38) -
Published as DNAJC19(NM_001190233.1):c.210A>C (p.G70=)
ISCN -
DB-ID DNAJC19_000005
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) 0.00499 View details
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 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FXR1 NM_005087.3 -?/. - c.*8414T>G r.(=) p.(=)
DNAJC19 NM_145261.3 -?/. - c.285A>C r.(?) p.(Gly95=)


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