rs46101708 SNP Detail

Summary

• ID
  rs46101708
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr10:13080409 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        GCATAGGTTT CTTTTCATGT CTCCTCTCAT CTATGACTTT
  GTCCTGGAGC TGAGAGAAGC CAAATTACTC CTTTAATCCC TCCCTTGAGG AATTTAAACC
  Y
  CTTTCTGGTT AAAATGTGCT CCCAGCTTTT TTTCTCTTGC TTACAGTGCA TTAAAAACTA
  AACACAATGA AGAACTCTAT TTCTTACTTT ATTAATTCT                       
  
  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	129X1/SvJ	A/J	DBA/2J
ss146812731	ENSMUSSNP5270313	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	C	T
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J	DBA/2J
rs46101708					SNP	C	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr10:13080409 () rs orientation: forward

Symbol	Name	Function Class
Gm47402	predicted gene, 47402	561 bp upstream