Product Details

SNP ID

rs76547503

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:43307628 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGCCTTACTTTTCTTGCCTTGGGG[A/G]AGGCCAGTCCTTGGCCTGGGAGGGC

Phenotype

MIM: 604995

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CRIP3 PubMed Links

Additional Information

For this assay, SNP(s) [rs148395811] 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

CRIP3

Gene Name

cysteine rich protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_206922.2	312	Silent Mutation	CTC,CTT	L104L	NP_996805.2
XM_005249103.3	312	Silent Mutation	CTC,CTT	L104L	XP_005249160.1
XM_011514609.2	312	Silent Mutation	CTC,CTT	L104L	XP_011512911.1
XM_017010856.1	312	Intron			XP_016866345.1
XM_017010857.1	312	Intron			XP_016866346.1

Gene

SLC22A7

Gene Name

solute carrier family 22 member 7

There are no transcripts associated with this gene.

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