Variant #0000567081 (NC_000019.9:g.3770844dup, NM_032753.3:c.335dup (RAX2))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3770844dup
DNA change (hg38) g.3770846dup
Published as RAX2(NM_001319074.1):c.473dupC (p.A159Gfs*178)
ISCN -
DB-ID MRPL54_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 10:06:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAX2 NM_032753.3 +/. - c.335dup r.(?) p.(Ala113GlyfsTer178)
MRPL54 NM_172251.2 +/. - c.*3453dup r.(?) p.(=)


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