Variant #0000336259 (NC_000023.10:g.153716736C>T, NM_014235.3:c.-1813G>A (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.153716736C>T
DNA change (hg38) g.154488397C>T
Published as SLC10A3(NM_001142391.2):c.457G>A (p.(Ala153Thr)), SLC10A3(NM_019848.4):c.544G>A (p.A182T), SLC10A3(NM_019848.5):c.544G>A (p.A182T)
ISCN -
DB-ID SLC10A3_000003 See all 4 reported entries
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) 0.00046 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-1813G>A r.(?) p.(=)
SLC10A3 NM_019848.3 ?/. - c.544G>A r.(?) p.(Ala182Thr)


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