Variant #0000566836 (NC_000019.9:g.33355112G>A, NM_001126335.1:c.368C>T (SLC7A9))

Chromosome 19
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.33355112G>A
DNA change (hg38) g.32864206G>A
Published as SLC7A9(NM_001126335.1):c.368C>T (p.(Thr123Met)), SLC7A9(NM_001243036.1):c.368C>T (p.T123M)
ISCN -
DB-ID SLC7A9_000023 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) 0.00019 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A9 NM_001126335.1 ?/. - c.368C>T r.(?) p.(Thr123Met)


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