Variant #0001050273 (NC_000001.10:g.154202194C>T, NC_000001.10(NM_014847.3):c.279+993C>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.154202194C>T
DNA change (hg38) -
Published as UBAP2L(NM_014847.4):c.279+993C>T
ISCN -
DB-ID C1orf43_000022
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBAP2L NM_014847.3 -?/. - c.279+993C>T r.(=) p.(=)
C1orf43 NM_015449.2 -?/. - c.-9311G>A r.(?) p.(=)


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