Variant #0000913148 (NC_000009.11:g.34241785C>T, NM_001171201.1:c.954C>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.34241785C>T
DNA change (hg38) -
Published as UBAP1(NM_001171201.1):c.954C>T (p.L318=)
ISCN -
DB-ID KIF24_000009
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +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     
UBAP1 NM_001171201.1 -?/. - c.954C>T r.(?) p.(Leu318=)
UBAP1 NM_016525.4 -?/. - c.762C>T r.(?) p.(Leu254=)
KIF24 NM_194313.2 -?/. - c.*12593G>A r.(=) p.(=)


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