Product Details

SNP ID

rs121909598

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:208121728 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCCACTCTGGCATTCGTGGCCCCC[T/C]AGTCCTGGTAGCGCCTATAGTCCCC

Phenotype

MIM: 123680 MIM: 123690

Polymorphism

T/C, Transition Substitution

Allele Nomenclature

Literature Links

CRYGC PubMed Links

Additional Information

For this assay, SNP(s) [rs2305429] 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

CRYGC

Gene Name

crystallin gamma C

There are no transcripts associated with this gene.

Gene

CRYGD

Gene Name

crystallin gamma D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006891.3	586	Nonsense Mutation	TAG,TGG	*157W	NP_008822.2

Gene

LOC100507443

Gene Name

uncharacterized LOC100507443

There are no transcripts associated with this gene.

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