Product Details

SNP ID

rs6118469

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:9075173 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATCCCAGGATGTTAAAGTTAGAA[C/T]TGAGACTGAAACTCAGGTAGGCTGA

Phenotype

MIM: 600810

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PLCB4 PubMed Links

Additional Information

For this assay, SNP(s) [rs74391622] 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

PLCB4

Gene Name

phospholipase C beta 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000933.3		Intron			NP_000924.3
NM_001172646.1		Intron			NP_001166117.1
NM_182797.2		Intron			NP_877949.2
XM_005260724.2		Intron			XP_005260781.1
XM_005260728.2		Intron			XP_005260785.1
XM_006723568.3		Intron			XP_006723631.1
XM_006723569.2		Intron			XP_006723632.1
XM_011529254.2		Intron			XP_011527556.1
XM_017027880.1		Intron			XP_016883369.1
XM_017027881.1		Intron			XP_016883370.1
XM_017027882.1		Intron			XP_016883371.1
XM_017027883.1		Intron			XP_016883372.1
XM_017027884.1		Intron			XP_016883373.1
XM_017027885.1		Intron			XP_016883374.1
XM_017027886.1		Intron			XP_016883375.1

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