Product Details

SNP ID

rs2707634

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99245387 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCACGCAATGTCTCTGCCCGACTT[C/T]TTTGATCAGAGTCTGGTAAGGTTTT

Phenotype

MIM: 616547

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LYG2 PubMed Links

Gene Details

Gene

LYG2

Gene Name

lysozyme g2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175735.3	369	Missense Mutation	AAA,GAA	K86E	NP_783862.2
XM_017003751.1	369	Missense Mutation	AAA,GAA	K86E	XP_016859240.1

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