Product Details

SNP ID

rs28616098

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:182447970 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCAGACCTAGAAGCTCTGAAATTT[A/T]AAAAAAAAAAAAAAAGCATTTTACC

Phenotype

MIM: 611012

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

RGSL1 PubMed Links

Additional Information

For this assay, SNP(s) [rs558278159] 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	94	Intron			NP_001131141.1
XM_005245137.1	94	Intron			XP_005245194.1
XM_011509494.2	94	Intron			XP_011507796.1
XM_011509496.1	94	Intron			XP_011507798.1
XM_011509500.1	94	Intron			XP_011507802.1
XM_011509503.1	94	Intron			XP_011507805.1
XM_011509504.2	94	Intron			XP_011507806.1
XM_017001188.1	94	Intron			XP_016856677.1
XM_017001189.1	94	Intron			XP_016856678.1
XM_017001190.1	94	Intron			XP_016856679.1
XM_017001191.1	94	Intron			XP_016856680.1
XM_017001192.1	94	Intron			XP_016856681.1
XM_017001193.1	94	UTR 5			XP_016856682.1
XM_017001194.1	94	Intron			XP_016856683.1
XM_017001195.1	94	Intron			XP_016856684.1
XM_017001196.1	94	Intron			XP_016856685.1
XM_017001197.1	94	Intron			XP_016856686.1

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