Variant #0000804097 (NC_000009.11:g.34241601C>T, NM_001171201.1:c.770C>T (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.34241601C>T
DNA change (hg38) -
Published as UBAP1(NM_001171203.2):c.578C>T (p.A193V)
ISCN -
DB-ID KIF24_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBAP1 NM_001171201.1 ?/. - c.770C>T r.(?) p.(Ala257Val)
UBAP1 NM_016525.4 ?/. - c.578C>T r.(?) p.(Ala193Val)
KIF24 NM_194313.2 ?/. - c.*12777G>A r.(=) p.(=)


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