Product Details

SNP ID

rs184303479

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:146194423 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCTGTGTCTCTCTATCTTGAACG[C/T]TGTGGTGGAGATCTTTCAAAATACA

Phenotype

MIM: 607612

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLSCR4 PubMed Links

Additional Information

For this assay, SNP(s) [rs1512902] 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

PLSCR4

Gene Name

phospholipid scramblase 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128304.1	1219	Silent Mutation	CAA,CAG	Q326Q	NP_001121776.1
NM_001128305.1	1219	Silent Mutation	CAA,CAG	Q326Q	NP_001121777.1
NM_001128306.1	1219	Silent Mutation	CAA,CAG	Q236Q	NP_001121778.1
NM_001177304.1	1219	Silent Mutation	CAA,CAG	Q221Q	NP_001170775.1
NM_020353.2	1219	Silent Mutation	CAA,CAG	Q326Q	NP_065086.2
XM_005247654.2	1219	Silent Mutation	CAA,CAG	Q326Q	XP_005247711.1
XM_005247655.2	1219	Silent Mutation	CAA,CAG	Q326Q	XP_005247712.1
XM_011513031.2	1219	Silent Mutation	CAA,CAG	Q326Q	XP_011511333.1
XM_017006921.1	1219	Silent Mutation	CAA,CAG	Q236Q	XP_016862410.1

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