Product Details

SNP ID

rs10252902

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:151434725 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGTCCTCACTTAACACCGTCAGTA[A/G]GTTCTTGGGAACCGTGGCTTTAAGC

Phenotype

MIM: 609603

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CRYGN PubMed Links

Additional Information

For this assay, SNP(s) [rs77114834] 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

CRYGN

Gene Name

crystallin gamma N

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308292.1		Intron			NP_001295221.1
NM_144727.2		Intron			NP_653328.1
XM_005249952.3		Intron			XP_005250009.1
XM_011515836.1		Intron			XP_011514138.1
XM_011515837.2		Intron			XP_011514139.1
XM_017011773.1		Intron			XP_016867262.1

Gene

MIR3907

Gene Name

microRNA 3907

There are no transcripts associated with this gene.

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