rs32127790 SNP Detail

Summary

• ID
  rs32127790
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  125
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr6:139438589 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AATATGTTGC CACCAGTGTC TGCAGAACTT TAACGAGAAG
  CAGATATATC CCAATTATTC TACTTAGTAG GCATCCAAAA TAAGTGTCAC CAGGGCAGTA
  R
  ATGTGTGGGA AGCATGAAGA CACTGAGTTT CTAAAGAGAT CATATTACCT TCACAACGTC
  CCGGAGGACA GTTTTATAGA CACTGGAAAT TCAAATAAAA                      
  
  R = A/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	129S1/SvImJ	BTBR T<+> Itpr3/J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
ss48128533	NES11845139	PERLEGEN	MM_PANEL2	f	SNP	G	G	G	G	A	G	G	G
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	BTBR T<+> Itpr3/J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	WSB/EiJ
rs32127790					SNP	G	G	G	G	A	G	G	G

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
ss48128533	NES11845139	PERLEGEN	MM_PANEL	f	SNP	A/G