rs37109741 SNP Detail

Summary

• ID
  rs37109741
• Variation Type
  SNP
• Alleles
  G/T

• Created in dbSNP Build
  126
• Last Updated in dbSNP Build
  137
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser | Alliance Variant
  

Genome Location and Flanking Sequence

• Location
  Chr1:162163944 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        ATACCCCCAG CTCTCTTTTT ATGTTCCTTT CTTTCCTTTC
  CTTTTCTTTT CTTTTCTTTC CTTTTTTTTT CTTTTCTTTG TCACTTTTAG ACAGTCTCCC
  K
  TAGCTCCACC AGCTGGCTGG TCTTTAGTTC ATTCTGTCAC CCAGGCAGGC CTTGAATTAT
  GATCCTCCTG CCTGAACCTC CAATCAGTTG GACTTACCT                       
  
  K = G/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	AKR/J	BTBR T<+> Itpr3/J	CAST/EiJ	DBA/2J	MOLF/EiJ	PWD/PhJ	WSB/EiJ
ss51399130	NES14460612	PERLEGEN	MM_PANEL2	f	SNP	G	G	T	T	T	G	G
SNP Consensus Information
SNP					Consensus Type	AKR/J	BTBR T<+> Itpr3/J	CAST/EiJ	DBA/2J	MOLF/EiJ	PWD/PhJ	WSB/EiJ
rs37109741					SNP	G	G	T	T	T	G	G

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
ss51399130	NES14460612	PERLEGEN	MM_PANEL	f	SNP	G/T

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:162163944 () rs orientation: forward

Symbol	Name	Transcript	Protein	Function Class	Allele	Residue	Codon Position	AA Position
Dnm3	dynamin 3			Intron
				Noncoding-Transcript-Variant
Rr421955	regulatory region 421955			1380 bp distal
Rr421956	regulatory region 421956			within coordinates
Rr421957	regulatory region 421957			196 bp proximal
Rr421958	regulatory region 421958			440 bp proximal