rs50985651 SNP Detail

Summary

• ID
  rs50985651
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  142
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr7:19117317 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                        GAGGG TAGAGTTGGT TCTTTCCTTC
  Y
  GTGTATGTCT TGGGGATTGA ACTCG                                      
  
  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	A/J	DBA/2J	LG/J	SM/J
ss148474265	ENSMUSSNP1719000	ENSEMBL	ENSEMBL_Sanger	f	SNP	C	T
ss322117091	CHEV_7_19968741	CHEVERUD	SCREENING_POP	f	SNP			C	T
SNP Consensus Information
SNP					Consensus Type	A/J	DBA/2J	LG/J	SM/J
rs50985651					SNP	C	T	C	T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr7:19117317 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Cpgi18481	CpG island 18481			732 bp distal
Ercc2	excision repair cross-complementing rodent repair deficiency, complementation group 2			Intron
				Noncoding-Transcript-Variant
Gm26852	predicted gene, 26852			within coordinates
Rr400148	regulatory region 400148			1303 bp downstream
Rr643124	regulatory region 643124			1342 bp distal
Rr643125	regulatory region 643125			1374 bp distal
Tssr64844	transcription start site region 64844			1340 bp downstream