Variant #0000692775 (NC_000019.9:g.3771688G>A, NM_032753.3:c.53C>T (RAX2))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3771688G>A
DNA change (hg38) -
Published as RAX2(NM_001319074.1):c.191C>T (p.P64L)
ISCN -
DB-ID MRPL54_000008
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAX2 NM_032753.3 ?/. - c.53C>T r.(?) p.(Pro18Leu)
MRPL54 NM_172251.2 ?/. - c.*4297G>A r.(=) p.(=)


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