All variants in the HEXA gene

Information The variants shown are described using the NM_000520.4 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.759G>A r.(?) p.(Val253=) - benign g.72642905C>T g.72350564C>T HEXA(NM_000520.5):c.759G>A (p.V253=), HEXA(NM_000520.6):c.759G>A (p.V253=) - HEXA_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-?/. - c.759G>A r.(?) p.(Val253=) - likely benign g.72642905C>T g.72350564C>T HEXA(NM_000520.5):c.759G>A (p.V253=), HEXA(NM_000520.6):c.759G>A (p.V253=) - HEXA_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
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