rs108841213 SNP Detail

Summary

• ID
  rs108841213
• Variation Type
  SNP
• Alleles
  A

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  ChrX:33423671 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GCAATTATTT TTATCTTAGA ATTCGTACAC AACTTACTCT
  TGTTTCTCAG TTGTTGTATG TTCAAATTCA TATCTTGAGA TCACAGAAAA TAATTTGGTT
  A
  TACGGGAAAT GGTAGAAAAA AAATTTGGGT CTGACTATTT CAATTTCCTC CTGTCAAATG
  AAAAGGCAAA TGCTACCTCT AAATACATAT CTTTGTGAAA A                    
  
  A = A
  

  
  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
ss134155255	ENSMUSSNP1669689	ENSEMBL	ENSEMBL_Sanger	f	SNP	A	A
SNP Consensus Information
SNP					Consensus Type	129X1/SvJ	A/J
rs108841213					SNP	A	A

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: ChrX:33423671 () rs orientation: forward

Symbol	Name	Function Class
Gm21870	predicted gene, 21870	192 bp upstream
Gm61620	predicted gene, 61620	within coordinates
Gm61788	predicted gene, 61788	within coordinates