Variant #0000567082 (NC_000019.9:g.3772023_3772024dup, NC_000019.9(NM_032753.3):c.-10+150_-10+151dup (RAX2))

Chromosome 19
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.3772023_3772024dup
DNA change (hg38) g.3772025_3772026dup
Published as RAX2(NM_001319074.1):c.-130-3_-130-2dupCA
ISCN -
DB-ID MRPL54_000004
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAX2 NM_032753.3 -?/. - c.-10+150_-10+151dup r.(=) p.(=)
MRPL54 NM_172251.2 -?/. - c.*4632_*4633dup r.(=) p.(=)


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