Variant #0000653772 (NC_000001.10:g.154247881C>T, NM_014847.3:c.*5110C>T (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.154247881C>T
DNA change (hg38) g.154275405C>T
Published as HAX1(NM_006118.3):c.676C>T (p.R226C)
ISCN -
DB-ID C1orf43_000008
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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +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     
HAX1 NM_006118.3 ?/. - c.676C>T r.(?) p.(Arg226Cys)
UBAP2L NM_014847.3 ?/. - c.*5110C>T r.(=) p.(=)
C1orf43 NM_015449.2 ?/. - c.-54998G>A r.(?) p.(=)


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