Variant #0000973341 (NC_000001.10:g.154245965A>T, NM_014847.3:c.*3194A>T (UBAP2L))

Chromosome 1
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.154245965A>T
DNA change (hg38) -
Published as HAX1(NM_006118.3):c.207A>T (p.P69=), HAX1(NM_006118.4):c.207A>T (p.(Pro69=))
ISCN -
DB-ID C1orf43_000003 See all 3 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) 0.00257 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 20:20:39 +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     
HAX1 NM_006118.3 -?/. - c.207A>T r.(?) p.(Pro69=)
UBAP2L NM_014847.3 -?/. - c.*3194A>T r.(=) p.(=)
C1orf43 NM_015449.2 -?/. - c.-53082T>A r.(?) p.(=)


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