Variant #0000990362 (NC_000001.10:g.154245875_154245880dup, NM_014847.3:c.*3104_*3109dup (UBAP2L))

Chromosome 1
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.154245875_154245880dup
DNA change (hg38) -
Published as HAX1(NM_006118.3):c.117_122dupAGAAGG (p.(Gly41_Gly42insGluGly)), HAX1(NM_006118.4):c.117_122dupAGAAGG (p.E40_G41dup)
ISCN -
DB-ID C1orf43_000001 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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.117_122dup r.(?) p.(Glu40_Gly41dup)
UBAP2L NM_014847.3 ?/. - c.*3104_*3109dup r.(=) p.(=)
C1orf43 NM_015449.2 ?/. - c.-52997_-52992dup r.(?) p.(=)


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