rs49769033 SNP Detail

Summary

• ID
  rs49769033
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr6:97835826 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TATTTTAACT CCATTTAAAA
  GAGTATTGAA GTACTTTCTA TGTGCATATT TTGCTTTTGT TCTAGTTTTG TTCCCATCTC
  CAAGCTCATT CAAGTCTTTA ACATTTCTAA GTTGCTAATG GACCTTCTGC AATCCTTGAA
  TTTGGTCCAT CTGGGCTATC CCGTGCCATT TCTTGATCTC AAAACTTTCA TCCTTTGCCT
  Y
  AGGTGCTTGT TTACTGATCA TGGCTGTCCT GTGTGTCAGA GTATACCTCA GAATATCCCT
  GTCCAGTGTG TATCTAACCC CCACCCAGTG GGGTGGTCCA CAGTATCTCT CTAGATATGC
  CAACATACTC TTCAGGGTTG GAGATGATCC TGGTTGAGAA GGAGCATCAT CTGCTGTGAT
  GTGTATCAAG TGTACTTTAT                                            
  
  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
ss60915467	NES16223103	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
rs49769033					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
ss60915467	NES16223103	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr6:97835826 () rs orientation: forward

Symbol	Name	Function Class
Mitf	melanogenesis associated transcription factor	Intron
Rr635230	regulatory region 635230	837 bp distal