Product Details

SNP ID

rs34443578

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99244074 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAATTCTCTCTGTTAGAATCCCAG[C/T]AGCCTGTGAAAGGTGCTCTTTGCTA

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	558	Missense Mutation	ACT,GCT	T149A	NP_783862.2
XM_017003751.1	558	Missense Mutation	ACT,GCT	T149A	XP_016859240.1

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