Variant #0000566835 (NC_000019.9:g.33353427C>T, NM_001126335.1:c.544G>A (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.33353427C>T
DNA change (hg38) g.32862521C>T
Published as SLC7A9(NM_001243036.1):c.544G>A (p.A182T), SLC7A9(NM_014270.5):c.544G>A (p.(Ala182Thr), p.A182T)
ISCN -
DB-ID SLC7A9_000032 See all 6 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) 0.00257 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 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A9 NM_001126335.1 ?/. - c.544G>A r.(?) p.(Ala182Thr)


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