Product Details

SNP ID

rs11068274

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.12:109786369 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ATGCTCTAAAATGAACCCACCATCC[A/G]AGTCTCTGCTTCCCCCTGAGCAAGA

Phenotype

MIM: 605427

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TRPV4 PubMed Links

Additional Information

For this assay, SNP(s) [rs114828827] 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

TRPV4

Gene Name

transient receptor potential cation channel subfamily V member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177428.1		Intron			NP_001170899.1
NM_001177431.1		Intron			NP_001170902.1
NM_001177433.1		Intron			NP_001170904.1
NM_021625.4		Intron			NP_067638.3
NM_147204.2		Intron			NP_671737.1
XM_005253918.1		Intron			XP_005253975.1
XM_011538630.2		Intron			XP_011536932.2
XM_011538631.2		Intron			XP_011536933.2
XM_011538632.2		Intron			XP_011536934.2
XM_011538633.2		Intron			XP_011536935.2
XM_011538634.2		Intron			XP_011536936.2
XM_011538635.2		Intron			XP_011536937.1
XM_011538636.2		Intron			XP_011536938.1
XM_017019774.1		Intron			XP_016875263.1

View Full Product Details