Variant #0000983091 (NC_000018.9:g.56936414G>T, NM_013435.2:c.863C>A (RAX))

Chromosome 18
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.56936414G>T
DNA change (hg38) -
Published as RAX(NM_013435.2):c.863C>A (p.P288Q), RAX(NM_013435.3):c.863C>A (p.(Pro288Gln))
ISCN -
DB-ID RAX_000021 See all 2 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) 0.00043 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
RAX NM_013435.2 ?/. - c.863C>A r.(?) p.(Pro288Gln)


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