Variant #0000516035 (NC_000002.11:g.44539792T>C, NM_000341.3:c.1400T>C (SLC3A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44539792T>C
DNA change (hg38) g.44312653T>C
Published as SLC3A1(NM_000341.3):c.1400T>C (p.M467T), SLC3A1(NM_000341.4):c.1400T>C (p.(Met467Thr), p.M467T)
ISCN -
DB-ID SLC3A1_000023 See all 3 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) 0.0025 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 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 +/. - c.1400T>C r.(?) p.(Met467Thr)
PREPL NM_006036.4 +/. - c.*8703A>G r.(=) p.(=)


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