rs30035264 SNP Detail

Summary

• ID
  rs30035264
• Variation Type
  SNP
• Alleles
  A/G

• Created in dbSNP Build
  125
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr13:25778598 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                                              TCAGCCAGTG ATTCCACTAA
  GCATTAATTC ATCAAATTAT CAAAATGACT TAACACAGTC TTAACCTAGT CATATTTATG
  AAAGTAAAAA TTTCTCTATT AAGTCATGTG AATTAGGAGG GGGGAGTGCC CTCAATCCTT
  TTGGTATCCT GAACGGCCAA GACCTCCCCC CCCCCCCCAT ACTGAGGACT TGTAAAACGG
  R
  AGAAACACCT TTGGGGAACT GTAAGGGTTT TTGAGTGAGC ATAGTAGCTC AGAAAACTCA
  TCAGTATGTA TTAAAACTGC ACAGGGAAAA CTGTCAGGCT TCTAGAGGCA AGTAACACAT
  CAAAGAGACA AACTACCCGC TGCCGGGGCT CAGGCTGACA TGAATATATA TCCAACTGTG
  GGAAATATGG CCAGACCCAA                                            
  
  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	LG/J	MOLF/EiJ	MSM/Ms	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
ss47406988	NES11358139	PERLEGEN	MM_PANEL2	f	SNP	A	A	A	A	A	A	A	A	A	G		G		G	A	G		A
ss148814766	ENSMUSSNP162256	ENSEMBL	ENSEMBL_Sanger	f	SNP		A						A					G
ss324304515	CHEV_13_25686484	CHEVERUD	SCREENING_POP	f	SNP											A						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	LG/J	MOLF/EiJ	MSM/Ms	NOD/ShiLtJ	NZW/LacJ	PWD/PhJ	SM/J	WSB/EiJ
rs30035264					SNP	A	A	A	A	A	A	A	A	A	G	A	G	G	G	A	G	G	A

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
ss47406988	NES11358139	PERLEGEN	MM_PANEL	f	SNP	A/G