rs49614618 SNP Detail

Summary

• ID
  rs49614618
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  127
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr17:19724752 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GCCTTTTCAT TTTTCAGTTA GTTGGACACC TGTGATGGAA
  ACTGTGGGGA TCAGCATAAC TTTTTTTTCA TATTAAAAGT TTCTTGCTTC ATATGGTTAG
  K
  CAATTCATCC CAAGAGAATA TCAACACTGA TCTCTTGCTG TTTGTAGTCT TTGATGAAGT
  CATAGTGCTT TTGTGTAGTG AAGAATATGA ACAAAATTAC                      
  
  K = G/T
  

  
  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	C3H/HeJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss60546300	NES16566025	PERLEGEN	MM_PANEL2	f	SNP	T	T	G	T	T	T	T
SNP Consensus Information
SNP					Consensus Type	C3H/HeJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs49614618					SNP	T	T	G	T	T	T	T

Additional submitted assays for this SNP, where the strain of origin for observed alleles is not specified by the submitter

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	Alleles
ss60546300	NES16566025	PERLEGEN	MM_PANEL	f	SNP	G/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr17:19724752 () rs orientation: forward

Symbol	Name	Function Class
Vmn2r100	vomeronasal 2, receptor 100	321 bp upstream