All variants in the SLC2A2 gene

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

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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.1403T>C r.(?) p.(Leu468Pro) - likely benign g.170715864A>G g.170998075A>G SLC2A2(NM_000340.1):c.1403T>C (p.(Leu468Pro)) - SLC2A2_000009 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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