Variant #0000503501 (NC_000001.10:g.154247434T>G, NM_014847.3:c.*4663T>G (UBAP2L))

Chromosome 1
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.154247434T>G
DNA change (hg38) g.154274958T>G
Published as HAX1(NM_001018837.1):c.369T>G (p.(Asp123Glu))
ISCN -
DB-ID C1orf43_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HAX1 NM_006118.3 ?/. - c.513T>G r.(?) p.(Asp171Glu)
UBAP2L NM_014847.3 ?/. - c.*4663T>G r.(=) p.(=)
C1orf43 NM_015449.2 ?/. - c.-54551A>C r.(?) p.(=)


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