rs49415633 SNP Detail

Summary

• ID
  rs49415633
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr1:3748619 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ATTCCCAGTA TTTTTGTCTC TACCCAGTGA TTTTACATTC
  ACCCAGAAAA CTTCTTCTCA CTTTTCAAGG ACCATATATA GTCCTCAGTT ACCCCAAATA
  M
  CATGTATATG CACAAGCTGT TTCATTGAAG GTTGTCTAAG AGAGCTGTTT CATTGAGTAT
  CAAATAAAAG AGCTGTTAGA GAAATGACAG AAGGAGCTG                       
  
  M = A/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	129X1/SvJ	A/J	DBA/2J
ss148459579	ENSMUSSNP2037077	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs49415633					SNP	C	C	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:3748619 () rs orientation: forward

Symbol	Name	Function Class
Gm10568	predicted gene 10568	1759 bp upstream