Product Details

SNP ID

rs111305526

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:81510801 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGCCAGGATGGAGCCACCGATCCA[C/G]ACCGAGTACTTGCGCTCTGGGGGTG

Phenotype

MIM: 102560 MIM: 607643

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ACTG1 PubMed Links

Additional Information

For this assay, SNP(s) [rs1139807] 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

ACTG1

Gene Name

actin gamma 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199954.1	1156	Silent Mutation	GTC,GTG	V339V	NP_001186883.1
NM_001614.3	1156	Silent Mutation	GTC,GTG	V339V	NP_001605.1

Gene

FSCN2

Gene Name

fascin actin-bundling protein 2, retinal

There are no transcripts associated with this gene.

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