rs28261230 SNP Detail

Summary

• ID
  rs28261230
• Variation Type
  SNP
• Alleles
  A/C

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

Genome Location and Flanking Sequence

• Location
  Chr2:174311880 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TCCCTTGGTC ATTCCCCGCT GTTTTTTCCA TGTCTGGCTT
  CTGCTCTGCA AAGGCCGCGC AATAGGAAAG GTGGAGGCCC TGATGACCTC CTTTAGCATG
  M
  TCACCTGCCT CCGGGAGCAA ACTGTGATTC TTCATCCAAC CCAGCTTGGA TTTTTCGGGG
  ACTTCGGAGG CACGACACAT GATTGGTGCT CAGGTGTGCA                      
  
  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	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss37829549	NES08708545	PERLEGEN	MM_PANEL2	f	SNP	A	A	A	A	A	A	C	A	A	C	A	C	A
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs28261230					SNP	A	A	A	A	A	A	C	A	A	C	A	C	A

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
ss37829549	NES08708545	PERLEGEN	MM_PANEL	f	SNP	A/C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:174311880 () rs orientation: forward

Symbol	Name	Function Class
Prelid3b	PRELI domain containing 3B	Intron
Rr572131	regulatory region 572131	106 bp proximal
Rr572132	regulatory region 572132	962 bp proximal
Rr572133	regulatory region 572133	1876 bp proximal