rs264643998 SNP Detail

Summary

• ID
  rs264643998
• Variation Type
  SNP
• Alleles
  C/G

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

Genome Location and Flanking Sequence

• Location
  Chr1:189087591 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                    GCTATAGTG TGCATTGTTT ATTCAAATAA
  ATTGCACAGG ATGTCAGCCA GCTGCGCTTT GGAGGACTGA TTTTAAAAAT CACTTTGTTT
  GTAGTGAGTT GAAATGCTAA ATATAAAAGT AAATTTTAAA ACATGTATAT CTCTCTCtgt
  S
  tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg tgtgtgtgtg taggtcagag acaactgtag
  gagtctgttc tatcctctta acatgtgggt tctgggaccc aaactcaggt catcagactt
  agtggcaagc actcttgcct aagagacatc                                 
  
  S = C/G
  

  
  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
ss320190786	CHEV_1_191179273	CHEVERUD	SCREENING_POP	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	LG/J	SM/J
rs264643998					SNP	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:189087591 () rs orientation: forward

Symbol	Name	Function Class
Kcnk2	potassium channel, subfamily K, member 2	Intron
Rr425789	regulatory region 425789	1099 bp distal