All transcript variants in gene CASR

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

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/? 4 c.514A>G r.(?) p.(R172G) ECD  - - g.121980396A>G g.122261549A>G - - CASR_000172 copied from CASRdb PubMed: Hinnie 2009 - - Germline - - - 0 - -
+/? 4 c.514A>G r.(?) p.(R172G) ECD  - - g.121980396A>G g.122261549A>G - - CASR_000172 copied from CASRdb Christie 2007 - - Germline - - - 0 - -
+/? 4 c.514A>G r.(?) p.(R172G) ECD  - - g.121980396A>G g.122261549A>G - - CASR_000172 copied from CASRdb Henn 2008 - - Germline - - - 0 - -
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