Variant #0000617568 (NC_000019.9:g.3771796dup, NC_000019.9(NM_032753.3):c.-9-41dup (RAX2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3771796dup
DNA change (hg38) g.3771798dup
Published as RAX2(NM_001319074.1):c.89dupC (p.A31Sfs*74)
ISCN -
DB-ID MRPL54_000007
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 2019-12-04 15:24:38 +01:00 (CET)
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.-9-41dup r.(=) p.(=)
MRPL54 NM_172251.2 +?/. - c.*4405dup r.(?) p.(=)


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