Product Details

SNP ID

rs16849482

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:73485038 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAGGAGATTGCTGTGTATTTGCAG[A/T]ATGTATACAGTATGCCCTATATGTT

Phenotype

MIM: 104145

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

AFM PubMed Links

Gene Details

Gene

AFM

Gene Name

afamin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001133.2		Intron			NP_001124.1
XM_017007842.1		Intron			XP_016863331.1
XM_017007843.1		Intron			XP_016863332.1
XM_017007844.1		Intron			XP_016863333.1

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