Variant #0000682287 (NC_000023.10:g.153714234_153714236del, NM_014235.3:c.242_244del (UBL4A))

Chromosome X
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.153714234_153714236del
DNA change (hg38) -
Published as UBL4A(NM_014235.5):c.242_244delAAG (p.E81del)
ISCN -
DB-ID SLC10A3_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) 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBL4A NM_014235.3 ?/. - c.242_244del r.(?) p.(Glu81del)
SLC10A3 NM_019848.3 ?/. - c.*1615_*1617del r.(=) p.(=)


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