Product Details

SNP ID

rs115813527

Assay Type

Functionally Tested

NCBI dbSNP Submissions

4

Location

Chr.1:153149896 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATGAATTCTAGTGATGTTACTTG[C/T]TCTTGGGTGGATACTTCTGCTGGCA

Phenotype

MIM: 182269

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SPRR2C PubMed Links

Additional Information

For this assay, SNP(s) [rs510277] 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

SPRR2C

Gene Name

small proline rich protein 2C (pseudogene)

There are no transcripts associated with this gene.

Gene

SPRR2G

Gene Name

small proline rich protein 2G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001014291.3	259	Missense Mutation	AAC,AGC	N72S	NP_001014313.1
XM_017002177.1	259	Missense Mutation	AAC,AGC	N72S	XP_016857666.1
XM_017002178.1	259	Missense Mutation	AAC,AGC	N72S	XP_016857667.1

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