Variant #0000931048 (NC_000019.9:g.3771586G>A, NM_032753.3:c.155C>T (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.3771586G>A
DNA change (hg38) -
Published as RAX2(NM_001319074.4):c.155C>T (p.P52L)
ISCN -
DB-ID MRPL54_000014
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) 0.01458 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAX2 NM_032753.3 -?/. - c.155C>T r.(?) p.(Pro52Leu)
MRPL54 NM_172251.2 -?/. - c.*4195G>A r.(=) p.(=)


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