Product Details

SNP ID

rs7771595

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:84136078 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTCTTAAGCAGCCATTCCTGCTTT[A/C]TTTGCTGACAAGGCCTTGATATTGT

Phenotype

MIM: 610201 MIM: 615410

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

CEP162 PubMed Links

Gene Details

Gene

CEP162

Gene Name

centrosomal protein 162

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286206.1		Intron			NP_001273135.1
NM_014895.3		Intron			NP_055710.2
XM_005248674.3		Intron			XP_005248731.1
XM_005248678.3		Intron			XP_005248735.1
XM_006715380.2		Intron			XP_006715443.1
XM_011535592.2		Intron			XP_011533894.1
XM_011535594.2		Intron			XP_011533896.1
XM_017010483.1		Intron			XP_016865972.1
XM_017010484.1		Intron			XP_016865973.1

Gene

MRAP2

Gene Name

melanocortin 2 receptor accessory protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138409.2		Intron			NP_612418.2
XM_011535400.2		Intron			XP_011533702.1
XM_017010219.1		Intron			XP_016865708.1
XM_017010220.1		Intron			XP_016865709.1
XM_017010221.1		Intron			XP_016865710.1

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