Variant #0000930662 (NC_000016.9:g.84066954A>T, NM_001080442.1:c.509T>A (SLC38A8))

Chromosome 16
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.84066954A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC38A8_000086
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC38A8 NM_001080442.1 ?/. - c.509T>A r.(?) p.(Ile170Asn)
SLC38A8 NM_001080442.3 ?/. - c.509T>A r.(?) p.(Ile170Asn)


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