Product Details

SNP ID

rs149488308

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:176083412 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCCCGGGGGAGCGAAGCGCGGAG[C/G]AGCCCACCTCCACGTCGCTGCTCAT

Phenotype

MIM: 142991 MIM: 142989

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

EVX2 PubMed Links

Gene Details

Gene

EVX2

Gene Name

even-skipped homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080458.1	551	Missense Mutation	TCC,TGC	S122C	NP_001073927.1

Gene

HOXD13

Gene Name

homeobox D13

There are no transcripts associated with this gene.

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