rs50751403 SNP Detail

Summary

• ID
  rs50751403
• 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
  Chr1:191709942 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        TCGGGCCTGA TCCTGAGGGT GCACAACCTG GTTTGTAAAC
  TTAGAGGAAG CCACATCTGT TGTCTACTTT GGGCAGAGCA AGCTTCTGAG AGAAACCAGC
  Y
  TTAACGTTCC CCCTTGTGCT GTGCAGGGGA CACAAGCAGG GGGAGAAAGC AGATCTAGAA
  TCAGAGGGGG CTACCTACCT GAGAAATGCA ACTTTAGCA                       
  
  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	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
ss60361406	NES15865157	PERLEGEN	MM_PANEL2	f	SNP	T	C	C	C	C	C	C	T	C	T		T	C	C	T		C
ss320196682	CHEV_1_193801862	CHEVERUD	SCREENING_POP	f	SNP											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	LG/J	MOLF/EiJ	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
rs50751403					SNP	T	C	C	C	C	C	C	T	C	T	T	T	C	C	T	C	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
ss60361406	NES15865157	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:191709942 () rs orientation: forward

Symbol	Name	Function Class
Gm70525	predicted gene, 70525	1640 bp downstream
Gm70534	predicted gene, 70534	within coordinates
Rd3	retinal degeneration 3	Intron
Rr426276	regulatory region 426276	598 bp distal
Rr426277	regulatory region 426277	416 bp distal
Rr426278	regulatory region 426278	1306 bp proximal
Tssr10797	transcription start site region 10797	592 bp downstream
Tssr10798	transcription start site region 10798	581 bp downstream
Tssr10799	transcription start site region 10799	536 bp downstream
Tssr10800	transcription start site region 10800	266 bp upstream
Tssr10801	transcription start site region 10801	303 bp upstream