rs30134762 SNP Detail

Summary

• ID
  rs30134762
• Variation Type
  SNP
• Alleles
  C/T

• 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
  Chr3:115808396 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              CTACTGGACC CAGGAGGATG
  GATAACCCAT AAGGCCTACC CTTGAATGAT TCTACTTCCT CTAGATAGAC CCCACTTCCT
  AAAGGCTCCA CAGTCGCCCT AAAGAGTGCC GCTACCTCTA GACTCAGTGT TCAGTCACAT
  GAACCTATGA AAGGCAGCTC AGGACCAAAC TGTAACAGTC ATGTAGGTGA GAATTTTGTC
  Y
  GCTTAAATTT GGTCAGTCAG ACACTTCCTA GTTAGTGTCT AGGAGGTAAG GACCTACTAA
  ACCTCTGGGG AAAGGATGAT GGTGTCTAAC AGATGGTGAA TTCCCACTCC CCCCACCCCC
  ACCCCCAGGA CAAATACGTT TGTTCACCAA GAGTTCCTGT AGAAACTGAG ATAGTAAAAA
  ATATTTCAAT TCAGAATAAC                                            
  
  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
ss46917003	NES10678519	PERLEGEN	MM_PANEL2	f	SNP	T	T	T	T	T	T	C	T	T	T	T	T	T	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
rs30134762					SNP	T	T	T	T	T	T	C	T	T	T	T	T	T	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
ss46917003	NES10678519	PERLEGEN	MM_PANEL	f	SNP	C/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr3:115808396 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Extl2	exostosin-like glycosyltransferase 2			Intron
				Noncoding-Transcript-Variant
Rr583640	regulatory region 583640			1290 bp proximal