All variants in the SLC2A2 gene

Information The variants shown are described using the NM_000340.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. - c.301G>A r.(?) p.(Val101Ile) - VUS g.170732328C>T g.171014539C>T SLC2A2(NM_000340.1):c.301G>A (p.(Val101Ile)) - SLC2A2_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.301G>A r.(?) p.(Val101Ile) - likely benign g.170732328C>T g.171014539C>T - - SLC2A2_000006 12 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs1800572 Germline - 12/2793 individuals - 0 - Mohammed Faruq
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