Product Details

SNP ID

rs1749459

Assay Type

Functionally Tested

NCBI dbSNP Submissions

33

Location

Chr.1:69574222 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCAATTATAGAAAAGAGGTAGCTG[A/T]CCTTAAAACAAAACAATAGCATAAA

Phenotype

MIM: 614453

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

LRRC7 PubMed Links

Additional Information

For this assay, SNP(s) [rs117790527] 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

LRRC7

Gene Name

leucine rich repeat containing 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020794.2		Intron			NP_065845.1
XM_017001885.1		Intron			XP_016857374.1
XM_017001886.1		Intron			XP_016857375.1
XM_017001887.1		Intron			XP_016857376.1
XM_017001888.1		Intron			XP_016857377.1
XM_017001889.1		Intron			XP_016857378.1
XM_017001890.1		Intron			XP_016857379.1
XM_017001891.1		Intron			XP_016857380.1
XM_017001892.1		Intron			XP_016857381.1
XM_017001893.1		Intron			XP_016857382.1
XM_017001894.1		Intron			XP_016857383.1
XM_017001895.1		Intron			XP_016857384.1

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