Product Details

SNP ID

rs1215499

Assay Type

Functionally Tested

NCBI dbSNP Submissions

23

Location

Chr.1:89632730 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGTGGTTTTCCGCGCATTGTGAGG[A/G]ATGAGGGGTGGAGGTGGTATTAGAC

Phenotype

MIM: 612889

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FLJ27354 PubMed Links

Additional Information

For this assay, SNP(s) [rs113690266] 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

FLJ27354

Gene Name

uncharacterized LOC400761

There are no transcripts associated with this gene.

Gene

LRRC8C

Gene Name

leucine rich repeat containing 8 family member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032270.4	30	Intron			NP_115646.2
XM_006710960.3	30	Intron			XP_006711023.1
XM_011542282.2	30	Intron			XP_011540584.1
XM_011542283.2	30	Intron			XP_011540585.1
XM_017002503.1	30	UTR 5			XP_016857992.1
XM_017002504.1	30	Intron			XP_016857993.1

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