Product Details

SNP ID

rs894738

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.12:54023741 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGTGTCAAATTTCACTTCTCTCCAT[A/G]CCTAAACTTTGAAAGGAGGAGTGTA

Phenotype

MIM: 142974 MIM: 142973 MIM: 142972

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HOXC4 PubMed Links

Additional Information

For this assay, SNP(s) [rs56394649] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

HOXC4

Gene Name

homeobox C4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014620.5		Intron			NP_055435.2
NM_153633.2		Intron			NP_705897.1

Gene

HOXC5

Gene Name

homeobox C5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018953.3		Intron			NP_061826.1

Gene

HOXC6

Gene Name

homeobox C6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004503.3		Intron			NP_004494.1
NM_153693.4		Intron			NP_710160.1

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