rs27959833 SNP Detail

Summary

• ID
  rs27959833
• Variation Type
  SNP
• Alleles
  C/G

• 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
  Chr2:70092194 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              GCGTTACAGC GCATGGTCAA
  TTGTTTCTGC TGGCTTGGTA CTGGGGTAGC ACCTAGTGGC AGGTTTGCCT GGTGGAGCAA
  AACCGTCTTT GTCTTGAGAG AAAGAAAATG GCCAGGTTTC CATCACTGCC TTTAGGGAGA
  CACTTCCACC AATCTGAAGA GCTCTCACTA GTTCCTGCCT CTTAGAGGCT TGCATCTCCT
  S
  CCAGTAGTAC CAGGGCTGGA GACTGTGCCT TGACACATGG GTCTTGGGGG GAGACTTTCC
  ACAACCAAGT TACCATGGTA ACTGCCATGT GACATCAGAG ATAGTAATCA CCCAGCATTT
  CCCCCAATGC TTCCTTTGAC TTTCCTGTTC TCACTGACTA TGAAAGAGAC TGAACATGCA
  GAGTGAAATA AAGCCCCAGG                                            
  
  S = C/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	129X1/SvJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	MSM/Ms	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
ss38127652	NES09288458	PERLEGEN	MM_PANEL2	f	SNP	C		C	C	C	C	C	G	C	C	C	G		C	C	G	C
ss146733397	ENSMUSSNP2393798	ENSEMBL	ENSEMBL_Sanger	f	SNP		C	C										G
SNP Consensus Information
SNP					Consensus Type	129S1/SvImJ	129X1/SvJ	A/J	AKR/J	BALB/cByJ	BTBR T<+> Itpr3/J	C3H/HeJ	CAST/EiJ	DBA/2J	FVB/NJ	KK/HlJ	MOLF/EiJ	MSM/Ms	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	WSB/EiJ
rs27959833					SNP	C	C	C	C	C	C	C	G	C	C	C	G	G	C	C	G	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
ss38127652	NES09288458	PERLEGEN	MM_PANEL	f	SNP	C/G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:70092194 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Myo3b	myosin IIIB			Intron
				Noncoding-Transcript-Variant
Rr558530	regulatory region 558530			1860 bp distal
Rr558531	regulatory region 558531			889 bp distal
Rr558532	regulatory region 558532			137 bp distal
Rr558533	regulatory region 558533			within coordinates
Rr558534	regulatory region 558534			646 bp proximal