Variant #0000726000 (NC_000016.9:g.84065530T>G, NM_001080442.1:c.574A>C (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.84065530T>G
DNA change (hg38) -
Published as SLC38A8(NM_001080442.2):c.574A>C (p.T192P), SLC38A8(NM_001080442.3):c.574A>C (p.T192P)
ISCN -
DB-ID SLC38A8_000010 See all 2 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) 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC38A8 NM_001080442.1 ?/. - c.574A>C r.(?) p.(Thr192Pro)


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