Product Details

SNP ID

rs200168432

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:49969699 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTGTCCTGCCAGCAACCCGCGGC[G/T]CTCTCTCAGCCCCTCTGCGGACCTG

Phenotype

MIM: 601911

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

DLX4 PubMed Links

Gene Details

Gene

DLX4

Gene Name

distal-less homeobox 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001934.3	155	Intron			NP_001925.2
NM_138281.2	155	Silent Mutation	GCG,GCT	A77A	NP_612138.1
XM_017024291.1	155	UTR 5			XP_016879780.1

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