Product Details

SNP ID

rs6663667

Assay Type

Functionally tested

NCBI dbSNP Submissions

29

Location

Chr.1:160680141 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCAACGTTCTCAGAGGCCAGAATCC[C/G]TGATGACTGGGCATGACAGGGGTCA

Phenotype

MIM: 109530

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CD48 PubMed Links

Gene Details

Gene

CD48

Gene Name

CD48 molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256030.1		Intron			NP_001242959.1
NM_001778.3		Intron			NP_001769.2
XM_005245625.1		Intron			XP_005245682.1
XM_011510171.1		Intron			XP_011508473.1
XM_017002867.1		Intron			XP_016858356.1

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