Variant #0000997841 (NC_000009.11:g.34179123G>T, NM_001171201.1:c.111G>T (UBAP1))

Chromosome 9
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.34179123G>T
DNA change (hg38) -
Published as UBAP1(NM_016525.4):c.-123G>T (p.?)
ISCN -
DB-ID KIF24_000013
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 13:16:32 +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     
UBAP1 NM_001171201.1 -?/. - c.111G>T r.(?) p.(Arg37Ser)
UBAP1 NM_016525.4 -?/. - c.-123G>T r.(?) p.(=)
KIF24 NM_194313.2 -?/. - c.*75255C>A r.(=) p.(=)


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