rs108643714 SNP Detail

Summary

• ID
  rs108643714
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  132
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr4:148333277 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        CATCAGTCAA CTACACCAAG ATCAGGTAAA GGCTGGACCC
  CTGCTTTCCA CACAGAGGCA GCAGGACATC TTGTCAAGCC TGAGAGGCTA AAGTGCCAGG
  C
  CTCAGGGAAG CCAGGTTAGG GGATATTGCC TGTGTGTATA CGTATGTACA TGTTTGTGTA
  CACATGTTCC TGTACCTTCT TTGGCAGAGC CACAGAAGA                       
  
  C = 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	A/J	LG/J	SM/J
ss147998430	ENSMUSSNP4462241	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
ss321418519	CHEV_4_147622929	CHEVERUD	SCREENING_POP	f	SNP		C	C
SNP Consensus Information
SNP					Consensus Type	A/J	LG/J	SM/J
rs108643714					SNP	C	C	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr4:148333277 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Disp3	dispatched RND transporter family member 3			Intron
				Noncoding-Transcript-Variant
Rr604634	regulatory region 604634			634 bp proximal
Rr604635	regulatory region 604635			699 bp proximal