Unique variants in gene NLRP13

Information The variants shown are described using the NM_176810.2 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
Legend  

Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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     
-?/. 1 - c.878A>G likely benign r.(?) p.(Asp293Gly) g.56424305T>C - NLRP13(NM_176810.2):c.878A>G (p.D293G) - NLRP13_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
Legend