rs50494768 SNP Detail

Summary

• ID
  rs50494768
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  127
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:194362148 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CCTGGCTGAA TGGAGGGAGG
  AAGCTGGCAC ATATGGTGGT AGACAGTGTT CCTCAGAGTT CAGTGGCAGG TGCTACTGTC
  TCTGGTGGCC CTCAACATCT CTATATTTGT TTCCTAAGAG GAAGAGTTTA AAGATTCAGG
  TCTGGAAGTT GGTATCTCTG GTCACAAGGC TGAGAGTTTG GAGATCTGTC ACCCTTCATA
  R
  CACACAGCAG GAGACACCAT AACACAAGCT GACCTACACA ATGGTCACTT GCTTTTCTTA
  TCTGTGACTT CTCATTCCTC TCATAACAGT CTTCCTTATA TCTATGCCTT GGTGCCTGAA
  CTAGCTCCTC ACACTTACTA TGAAGTGAGA TCTGGGCCCC AACCCATAGC CTGCCTCAAA
  CTACAGCAGA GTCTCCAAAG                                            
  
  R = A/G
  

  
  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
ss60363398	NES15868886	PERLEGEN	MM_PANEL2	f	SNP	G	G	G	G	G	G	G	G	G	G	A	G	G	G	G
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
rs50494768					SNP	G	G	G	G	G	G	G	G	G	G	A	G	G	G	G

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
ss60363398	NES15868886	PERLEGEN	MM_PANEL	f	SNP	A/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:194362148 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Gm38036	predicted gene, 38036			within coordinates
Gm46202	predicted gene, 46202			within coordinates
Plxna2	plexin A2			Intron
				Noncoding-Transcript-Variant
Rr426680	regulatory region 426680			1509 bp distal
Rr426681	regulatory region 426681			303 bp distal
Rr426682	regulatory region 426682			413 bp proximal