All variants in the HGSNAT gene

Information The variants shown are described using the NM_152419.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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.564-98T>C r.(=) p.(=) - benign g.43024218T>C g.43169075T>C - - HGSNAT_000092 - PubMed: Martins 2019, Journal: Martins 2019 - - Germline - - - 0 - Carla Martins
-/. - c.564-98T>C r.(=) p.(=) - benign g.43024218T>C g.43169075T>C - - HGSNAT_000092 - PubMed: Martins 2019, Journal: Martins 2019 - - Germline - - - 0 - Carla Martins
-/. - c.564-98T>C r.(=) p.(=) - benign g.43024218T>C g.43169075T>C - - HGSNAT_000092 - PubMed: Martins 2019, Journal: Martins 2019 - - Germline - - - 0 - Carla Martins
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