Variant #0000336258 (NC_000023.10:g.153716294A>G, NM_014235.3:c.-1371T>C (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.153716294A>G
DNA change (hg38) g.154487955A>G
Published as SLC10A3(NM_001142391.2):c.899T>C (p.(Phe300Ser))
ISCN -
DB-ID SLC10A3_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UBL4A NM_014235.3 ?/. - c.-1371T>C r.(?) p.(=)
SLC10A3 NM_019848.3 ?/. - c.986T>C r.(?) p.(Phe329Ser)


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