Product Details

SNP ID

rs141102051

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:186613340 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTTGAACCAGATTGATGAAGTA[A/G]AGGTGTGGCCTCAGGTAAGTGGACC

Phenotype

MIM: 138680

Polymorphism

A/G, Transition 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	413	Missense Mutation	AAG,GAG	K67E	NP_001613.2
XM_017005840.1	413	Missense Mutation	AAG,GAG	K67E	XP_016861329.1

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