Full data view for gene HGSNAT

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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 5 c.525dup r.(?) p.(Val176Cysfs*16) Parent #2 - pathogenic (recessive) g.43016612dup g.43161469dup - - HGSNAT_000087 2/11 MPSIIIC alleles in Paraiba, 2/23 MPSIIIC alleles in Brazil PubMed: Martins 2019, Journal: Martins 2019 - rs483352895 Germline - - - 0 - DNA SEQ - - MPS3C Br4 PubMed: Martins 2019, Journal: Martins 2019 origin: state of Paraiba F no Brazil - - 0 - - 1 Carla Martins
+?/. 5 c.525dup r.(?) p.(Val176Cysfs*16) Parent #1 - pathogenic (recessive) g.43016612dup g.43161469dup - - HGSNAT_000087 2/11 MPSIIIC alleles in Paraiba, 2/23 MPSIIIC alleles in Brazil PubMed: Martins 2019, Journal: Martins 2019 - rs483352895 Germline - - - 0 - DNA SEQ - - MPS3C Br5 PubMed: Martins 2019, Journal: Martins 2019 origin: state of Paraiba F no Brazil - 22y 0 - - 1 Carla Martins
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