C___9606820_30

• SNP ID: rs997218
• Gene: CMIP
• Gene Name: c-Maf inducing protein
• Set Membership: > HapMap
• Chromosome Location: Chr.16: 81563568 - 81563568 on Build GRCh38
• Polymorphism: T/C, Transition substitution
• Context Sequence [VIC/FAM]:

  GCATGTTTACAAAACCCCCAGGCGA[T/C]ACATGTGCACATTAAAGCTGAGACA

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:	MIM: 610112
Literature Links:	CMIP PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome	Applied Biosystems^®	HapMap
Global T (0.50) (0.50)	Caucasian - Not Available	CEPH (CEU) C (0.39) (0.61)
EAS C (0.44) (0.56)	African American - Not Available	YRI (Yoruba) T (0.19) (0.81)
SAS C (0.39) (0.61)	Chinese - Not Available	JPT (Japanese) C (0.44) (0.56)
AFR T (0.16) (0.84)	Japanese - Not Available	CHB (Han Chinese) C (0.45) (0.55)
EUR C (0.35) (0.65)
AMR C (0.35) (0.65)

CMIP - c-Maf inducing protein
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_030629.2		Intron			NP_085132.1
NM_198390.2		Intron			NP_938204.2
XM_005256179.4		Intron			XP_005256236.4
XM_005256181.2		Intron			XP_005256238.1
XM_005256182.1		Intron			XP_005256239.1
XM_011523352.1		Intron			XP_011521654.1
XM_011523353.1		Intron			XP_011521655.1
XM_017023733.1		Intron			XP_016879222.1

More Information

• Set Membership: HapMap

Gene Ontology Categories:

Function(s)

protein binding