Product Details

SNP ID

rs4831

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:186613180 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTGCTCCTTTGTCTTGCTCAGCT[C/G]TGGGGCTGCCACTCAGCCCCACATG

Phenotype

MIM: 138680

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

AHSG PubMed Links

Gene Details

Gene

AHSG

Gene Name

alpha 2-HS glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001622.2	253	Silent Mutation	CTC,CTG	L13L	NP_001613.2
XM_017005840.1	253	Silent Mutation	CTC,CTG	L13L	XP_016861329.1

View Full Product Details