rs37799638 SNP Detail

Summary

• ID
  rs37799638
• Variation Type
  SNP
• Alleles
  A/C

• Created in dbSNP Build
  126
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr6:98991844 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              ACCTACAGAA GATGAGGTGG
  GAACCCCTGC CTGGGAAGGT CCCATGGTGC ATGGTCCCTG GGAAGGTCTA CAAGGGTCAC
  CTGCATGGGC AGAGCAGCCA AATGAAATCA ATTAGAAACA CTGCAAAGAA CTGGGACACA
  GAAGTAAATA CAGTGTAGGG GGTGGGGGTT TGCTGCTGTT TAGCTTTGTT TTGCTAAGTA
  M
  AGGTGAGTCC CCTGACTTTA ACTCATGCAC ATGTGTTAGG CAATTAGGAC ACACTCACCA
  TGCAAGAGGC TAGATGAAGA TATCGGTGTT TAAGCACGTT CTAAACGCCT GGCTTGTCTA
  ACCTCACAAG AAGGTAGCTG GCCAATGGAG AAGGCCATTG CCACCTTCCC AAATGCTTGG
  GTTCATAAGG CAAACAAACC                                            
  
  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	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss51381393	NES13732171	PERLEGEN	MM_PANEL2	f	SNP	C	C	C	C	C	C	C	C	C	C	C	C	C	A	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
rs37799638					SNP	C	C	C	C	C	C	C	C	C	C	C	C	C	A	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
ss51381393	NES13732171	PERLEGEN	MM_PANEL	f	SNP	A/C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:98991844 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Foxp1	forkhead box P1			Intron
				Noncoding-Transcript-Variant
Rr406577	regulatory region 406577			282 bp distal
Rr635319	regulatory region 635319			282 bp distal