Product Details

SNP ID

rs61275549

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:70900676 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCCCCGCGCGCCGGGCGGAGTCT[A/G]GTGGCGGCGGTGGGCGCTGCGGAGA

Phenotype

MIM: 604295

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VAX2 PubMed Links

Gene Details

Gene

VAX2

Gene Name

ventral anterior homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012476.2	126	Missense Mutation	AGT,GGT	S19G	NP_036608.1
XM_006711982.3	126	Missense Mutation	AGT,GGT	S19G	XP_006712045.1
XM_011532750.2	126	Missense Mutation	AGT,GGT	S19G	XP_011531052.1
XM_011532751.2	126	Missense Mutation	AGT,GGT	S19G	XP_011531053.1

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