rs33194737 SNP Detail

Summary

• ID
  rs33194737
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:41655221 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              AGAAGGCAGT AGCATTATCT
  TATCTGGTTC ACTCACATTT TATTGCTTTC TCTCATTTCT CTTGAGCCCC TTCTCTAAGG
  ACCATTTGTT CCCTCTCTTC ATCTCCGAGT AAAGCTTGTT CTGTGTAGTG TTAAACATCC
  AGGATAGTCC TTTATTCCAA TCATCCTATC AAGTATTATT TTGGTCACTT TCTCAGGTAT
  Y
  TCCTTGACTC TTTGCTGGCA ATTGTCAGTG CCTTGATAAC ATCTACCTGC TTGGGCCTCC
  AAGCATCGAC CTCTCTATAT GAAAACTTGT GAAAGCATAA GGGAGGGACT AAGCTGTCTT
  TCTTATTGGG TCTTAAATTG ATCAATCACA TTAATTCCTT GATTTTTTTT TCTCAAAAGC
  AGCTTGTACA ATTCAGTTTG                                            
  
  Y = C/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	CAST/EiJ	MOLF/EiJ
ss47268347	NES11089410	PERLEGEN	MM_PANEL2	f	SNP	T	C
SNP Consensus Information
SNP					Consensus Type	CAST/EiJ	MOLF/EiJ
rs33194737					SNP	T	C

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
ss47268347	NES11089410	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:41655221 () rs orientation: forward

Symbol	Name	Function Class
Gm70758	predicted gene, 70758	1529 bp downstream