All variants in the SOX9 gene

Information The variants shown are described using the NM_000346.3 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.508C>G r.(?) p.(Pro170Ala) - likely pathogenic g.70118936C>G - - - SOX9_000045 - - - - Unknown - - - 0 - IMGAG
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