Product Details

SNP ID

rs148977203

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:798803 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGGAAGGGGTCCTTGGGGATCCC[A/G]TCCTCGATCCACTTCAGCAGCCTGC

Phenotype

MIM: 613201 MIM: 607298

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CHTF18 PubMed Links

Additional Information

For this assay, SNP(s) [rs36073541] 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

CHTF18

Gene Name

chromosome transmission fidelity factor 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022092.2	222	Intron			NP_071375.1
XM_005255470.1	222	Intron			XP_005255527.1
XM_005255471.3	222	Intron			XP_005255528.1
XM_011522572.1	222	Intron			XP_011520874.1
XM_011522573.1	222	Intron			XP_011520875.1
XM_017023532.1	222	Intron			XP_016879021.1
XM_017023533.1	222	Intron			XP_016879022.1
XM_017023534.1	222	Intron			XP_016879023.1

Gene

GNG13

Gene Name

G protein subunit gamma 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016541.2	222	Silent Mutation			NP_057625.1

Gene

PRR25

Gene Name

proline rich 25

There are no transcripts associated with this gene.

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