Variant #0000343431 (NC_000001.10:g.154246014C>T, NM_014847.3:c.*3243C>T (UBAP2L))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.154246014C>T
DNA change (hg38) g.154273538C>T
Published as HAX1(NM_006118.3):c.256C>T (p.R86*)
ISCN -
DB-ID HAX1_000005 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HAX1 NM_006118.3 +/. - c.256C>T r.(?) p.(Arg86Ter)
UBAP2L NM_014847.3 +/. - c.*3243C>T r.(=) p.(=)
C1orf43 NM_015449.2 +/. - c.-53131G>A r.(?) p.(=)


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