Variant #0000308377 (NC_000001.10:g.43408966G>A, NM_006516.2:c.45C>T (SLC2A1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43408966G>A
DNA change (hg38) g.42943295G>A
Published as SLC2A1(NM_006516.3):c.45C>T (p.A15=), SLC2A1(NM_006516.4):c.45C>T (p.A15=)
ISCN -
DB-ID SLC2A1_000034 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) 0.24165 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC2A1 NM_006516.2 -/. - c.45C>T r.(?) p.(Ala15=)


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