Product Details

SNP ID

rs4556322

Assay Type

Functionally Tested

NCBI dbSNP Submissions

2

Location

Chr.1:182451702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACTAGAGAGTTTGGACTTTACCTT[C/T]TAGGACATCAAGGAGATTTTGAAAG

Phenotype

MIM: 611012

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RGSL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs534168859] 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

RGSL1

Gene Name

regulator of G-protein signaling like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001137669.1		Intron			NP_001131141.1
XM_005245137.1		Intron			XP_005245194.1
XM_011509494.2		Intron			XP_011507796.1
XM_011509496.1		Intron			XP_011507798.1
XM_011509500.1		Intron			XP_011507802.1
XM_011509503.1		Intron			XP_011507805.1
XM_011509504.2		Intron			XP_011507806.1
XM_017001188.1		Intron			XP_016856677.1
XM_017001189.1		Intron			XP_016856678.1
XM_017001190.1		Intron			XP_016856679.1
XM_017001191.1		Intron			XP_016856680.1
XM_017001192.1		Intron			XP_016856681.1
XM_017001193.1		Intron			XP_016856682.1
XM_017001194.1		Intron			XP_016856683.1
XM_017001195.1		Intron			XP_016856684.1
XM_017001196.1		Intron			XP_016856685.1
XM_017001197.1		Intron			XP_016856686.1

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