All transcript variants in gene CASR

Information The variants shown are described using the NM_000388.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
+/? 3 c.346G>A r.(?) p.(A116T) ECD  - pathogenic g.121976088G>A g.122257241G>A - - CASR_000030 copied from CASRdb PubMed: Baron 1996 - - Germline - - - 0 - -
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