Full data view for gene ARSB

Information The variants shown are described using the NM_000046.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Clinical classification     

Allele     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Template     

Technique     

Disease     

Reference     

Gender     

Geographic origin     

Consanguinity     

Remarks     

Panel size     

Owner     
./. - c.982G>C r.(?) p.(Gly328Arg) likely pathogenic Both (homozygous) g.78181567C>G - ARSB_000017 DNA SEQ-NG MPS VI - F Iran yes - 1 Variome.ir
./. - c.982G>C r.(?) p.(Gly328Arg) likely pathogenic Both (homozygous) g.78181567C>G - ARSB_000017 DNA SEQ MPS VI - M Iran yes - 1 Variome.ir
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