Variant #0000295922 (NC_000016.9:g.84065476G>C, NM_001080442.1:c.628C>G (SLC38A8))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.84065476G>C
DNA change (hg38) g.84031871G>C
Published as SLC38A8(NM_001080442.2):c.628C>G (p.L210V), SLC38A8(NM_001080442.3):c.628C>G (p.L210V)
ISCN -
DB-ID SLC38A8_000009 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) 0.00071 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC38A8 NM_001080442.1 -/. - c.628C>G r.(?) p.(Leu210Val)


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