rs27195127 SNP Detail

Summary

• ID
  rs27195127
• Variation Type
  SNP
• Alleles
  C/T

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr2:31855065 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GGTAGAATTT TCCTCGTGGC
  TAATTCTTGC CTACCTGGTA TCAGGAGAAG TTTTTTGGCT CTTCCAGAGA CAACAGCTAA
  GACGACAGGA CCCCTTGGGC TGGGGAGGGT GTCAAGGGTT CCTCAAGGGT TCAGTCAGCC
  CTTTCTAGAG AGTCACTGGG CTCTGCAGGG AGAGCTGTGG CTTCTAATCT AATGGCAGTT
  Y
  GTGCTTGTGA TTTTCAGAGA AATACATGGA GTTTGACCTG AATAATGAAG GCGAGATTGG
  TGAGTGAGGC CTTGGTGGTG GAGAAGGAGG ATGGGAAGGA GGCCTGAGAG CCAAAGAATC
  CTGCTGCTCT GGGGAGGAGC ACTGGGTGAA GCTGAAGAAC ACCCAGATGC ATGAGGCCCT
  GATGGTCCTG GTGGCCAAGC                                            
  
  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	129S1/SvImJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss37400958	NES08755912	PERLEGEN	MM_PANEL2	f	SNP	C	C	C	C	C	C	C	C	C	C	T	C	C	T	C
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	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs27195127					SNP	C	C	C	C	C	C	C	C	C	C	T	C	C	T	C

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
ss37400958	NES08755912	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:31855065 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Aif1l	allograft inflammatory factor 1-like			Intron
				Noncoding-Transcript-Variant
Gm13442	predicted gene 13442			within coordinates
Rr554765	regulatory region 554765			1126 bp distal
Rr554766	regulatory region 554766			116 bp proximal
Rr554767	regulatory region 554767			236 bp proximal
Tssr459	transcription start site region 459			629 bp upstream