All transcript variants in gene G6PC2

Information The variants shown are described using the NM_021176.2 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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.620A>C likely benign r.(?) p.(Tyr207Ser) g.169764141A>C - G6PC2(NM_001081686.1):c.*39A>C (p.(=)) - G6PC2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-?/. - c.847C>T likely benign r.(?) p.(Arg283*) g.169764368C>T - G6PC2(NM_001081686.1):c.*266C>T (p.(=)) - G6PC2_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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