Variant #0000997843 (NC_000009.11:g.34249958A>G, NM_001171201.1:c.1457A>G (UBAP1))

Chromosome 9
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.34249958A>G
DNA change (hg38) -
Published as UBAP1(NM_016525.4):c.1265A>G (p.(Gln422Arg))
ISCN -
DB-ID KIF24_000015
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_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.1457A>G r.(?) p.(Gln486Arg)
UBAP1 NM_016525.4 ?/. - c.1265A>G r.(?) p.(Gln422Arg)
KIF24 NM_194313.2 ?/. - c.*4420T>C r.(=) p.(=)


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