Product Details

SNP ID

rs117987138

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:71743295 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATGGAAATGAAACACATAGCCAA[A/C]CAAAGTTGGCTTAATGGTTTTAGGA

Phenotype

MIM: 139200

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

GC PubMed Links

Gene Details

Gene

GC

Gene Name

GC, vitamin D binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000583.3		Intron			NP_000574.2
NM_001204306.1		Intron			NP_001191235.1
NM_001204307.1		Intron			NP_001191236.1
XM_006714177.2		Intron			XP_006714240.1

View Full Product Details