Product Details

SNP ID

rs199625462

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:30369514 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGATGCCCCCTGCACAGGCTGCG[A/G]GGCCCTGCATGTCCGTGGGGCTCAC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CCDC157 PubMed Links

Additional Information

For this assay, SNP(s) [rs5749080] 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

CCDC157

Gene Name

coiled-coil domain containing 157

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017437.3	654	Missense Mutation	AGG,GGG	R111G	NP_001017437.2
NM_001318334.1	654	Missense Mutation	AGG,GGG	R111G	NP_001305263.1
NM_001318335.1	654	Intron			NP_001305264.1
XM_006724278.3	654	Missense Mutation	AGG,GGG	R111G	XP_006724341.1
XM_006724279.3	654	Missense Mutation	AGG,GGG	R111G	XP_006724342.1
XM_006724280.3	654	Missense Mutation	AGG,GGG	R111G	XP_006724343.1
XM_011530263.2	654	Missense Mutation	AGG,GGG	R111G	XP_011528565.1
XM_011530266.2	654	Missense Mutation	AGG,GGG	R111G	XP_011528568.1
XM_011530267.2	654	Missense Mutation	AGG,GGG	R111G	XP_011528569.1
XM_011530268.2	654	Missense Mutation	AGG,GGG	R111G	XP_011528570.1
XM_011530269.2	654	Intron			XP_011528571.1
XM_011530270.2	654	Missense Mutation	AGG,GGG	R111G	XP_011528572.1

Gene

KIAA1656

Gene Name

KIAA1656 protein

There are no transcripts associated with this gene.

Gene

RNF215

Gene Name

ring finger protein 215

There are no transcripts associated with this gene.

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