rs218604732 SNP Detail

Summary

• ID
  rs218604732
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  137
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr6:118573890 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CATCACTGTG ACTCTCCACT GTCCACTGCT CAGATGTGAT
  ACGTTTGTTG AAAAGAATGG GACCCTTTGG GACCAAATGG TGGGAATGTC CATCCCGGGA
  C
  GACAGAGAGG ATGGGTTGGA GGTGCCAGAT CATACACAGG GGAAACTAGT TTCCTTCCTA
  TGGGCATGAG GACAGGTGGG CAAACCAACC TGGAGAAAC                       
  
  C = C
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	LG/J	SM/J
ss321925398	CHEV_6_118546947	CHEVERUD	SCREENING_POP	f	SNP	C	C
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs218604732					SNP	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:118573890 () rs orientation: forward

Symbol	Name	Function Class
Cacna1c	calcium channel, voltage-dependent, L type, alpha 1C subunit	within coordinates
Gm38887	predicted gene, 38887	within coordinates