Variant #0000888818 (NC_000009.11:g.34241449_34241450del, NM_001171201.1:c.618_619del (UBAP1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34241449_34241450del
DNA change (hg38) -
Published as UBAP1(NM_001171203.3):c.426_427delGA (p.K143Sfs*15)
ISCN -
DB-ID UBAP1_000004 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +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.618_619del r.(?) p.(Lys207Serfs*15)
UBAP1 NM_016525.4 +/. - c.426_427del r.(?) p.(Lys143Serfs*15)
KIF24 NM_194313.2 +/. - c.*12929_*12930del r.(=) p.(=)


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