Variant #0000163209 (NC_000001.10:g.43424429C>T, NM_006516.2:c.-107G>A (SLC2A1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.43424429C>T
DNA change (hg38) g.42958758C>T
Published as -
ISCN -
DB-ID SLC2A1_000036 See all 3 reported entries
Variant remarks cDNA expression cloning in HEK293T cells shows preferential translation initiation at new ATG
Reference Kamsteeg submitted
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Erik-Jan Kamsteeg
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-02-20 09:39:11 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC2A1 NM_006516.2 +/. 1 c.-107G>A r.(?) p.Met1extMet-36fs*44


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