Product Details

SNP ID

rs111668637

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:44612170 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCATGTCTGTCTGCTCCAGTGAC[A/G]TGGGCCATGTCAGCCGAGTCTCCTC

Phenotype

MIM: 612920

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

KRTAP10-7 PubMed Links

Additional Information

For this assay, SNP(s) [rs411254] are located under a probe 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

KRTAP10-7

Gene Name

keratin associated protein 10-7

There are no transcripts associated with this gene.

Gene

KRTAP10-8

Gene Name

keratin associated protein 10-8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198695.2	92	Missense Mutation	ATG,GTG	M24V	NP_941968.2

Gene

TSPEAR

Gene Name

thrombospondin type laminin G domain and EAR repeats

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001272037.1	92	Intron			NP_001258966.1
NM_144991.2	92	Intron			NP_659428.2

View Full Product Details