Variant #0000437132 (NC_000011.9:g.118898998C>T, NM_001164277.1:c.287G>A (SLC37A4))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.118898998C>T
DNA change (hg38) g.119028288C>T
Published as -
ISCN -
DB-ID SLC37A4_000033 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121908976
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-01-21 14:16:04 +01:00 (CET)
Date last edited 2021-09-09 14:41:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC37A4 NM_001164277.1 ?/? 4 c.287G>A r.(?) p.(Trp96*)


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