Product Details

SNP ID

rs148151655

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:92424711 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACAAATGCTCCTTTCATTCCTCT[A/G]TTTACAGACCTGCCGCAGACAATTC

Phenotype

MIM: 616988 MIM: 616989

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CLLU1 PubMed Links

Additional Information

For this assay, SNP(s) [rs12580153] 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

CLLU1

Gene Name

chronic lymphocytic leukemia up-regulated 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025233.2	753	Missense Mutation	ATT,GTT	I11V	NP_001020404.1

Gene

CLLU1OS

Gene Name

chronic lymphocytic leukemia up-regulated 1 opposite strand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001025232.1	753	Intron			NP_001020403.1
XM_017019673.1	753	Intron			XP_016875162.1

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