Product Details

SNP ID

rs35389724

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:128901376 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACGTGTAAGGCACCCAGTCCAGAG[C/T]AGTGCACGCAAACACACACACACAC

Phenotype

MIM: 600734

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

C11orf45 PubMed Links

Additional Information

For this assay, SNP(s) [rs144517706] 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

C11orf45

Gene Name

chromosome 11 open reading frame 45

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256088.1	1813	UTR 3			NP_001243017.1
NM_145013.2	1813	UTR 3			NP_659450.1
XM_011542654.2	1813	UTR 3			XP_011540956.1
XM_011542655.2	1813	UTR 3			XP_011540957.1

Gene

KCNJ5

Gene Name

potassium voltage-gated channel subfamily J member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000890.3	1813	Intron			NP_000881.3
XM_011542809.2	1813	Intron			XP_011541111.1
XM_011542810.2	1813	Intron			XP_011541112.1

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