Product Details

SNP ID

rs28558201

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:71934453 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTCTGGCAGATCTTAACTTTACTT[C/G]TGATTTTCTTTAAGGAATTTCAGTT

Phenotype

MIM: 603894

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RGS6 PubMed Links

Gene Details

Gene

RGS6

Gene Name

regulator of G-protein signaling 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204416.2		Intron			NP_001191345.1
NM_001204417.2		Intron			NP_001191346.1
NM_001204418.2		Intron			NP_001191347.1
NM_001204419.2		Intron			NP_001191348.1
NM_001204420.2		Intron			NP_001191349.1
NM_001204421.2		Intron			NP_001191350.1
NM_001204422.2		Intron			NP_001191351.1
NM_001204423.1		Intron			NP_001191352.1
NM_001204424.1		Intron			NP_001191353.1
NM_004296.6		Intron			NP_004287.3
XM_011537393.2		Intron			XP_011535695.1
XM_011537397.1		Intron			XP_011535699.1
XM_011537407.2		Intron			XP_011535709.1
XM_017021818.1		Intron			XP_016877307.1
XM_017021819.1		Intron			XP_016877308.1
XM_017021820.1		Intron			XP_016877309.1
XM_017021821.1		Intron			XP_016877310.1
XM_017021822.1		Intron			XP_016877311.1
XM_017021823.1		Intron			XP_016877312.1
XM_017021824.1		Intron			XP_016877313.1
XM_017021825.1		Intron			XP_016877314.1
XM_017021826.1		Intron			XP_016877315.1
XM_017021827.1		Intron			XP_016877316.1
XM_017021828.1		Intron			XP_016877317.1
XM_017021829.1		Intron			XP_016877318.1
XM_017021830.1		Intron			XP_016877319.1
XM_017021831.1		Intron			XP_016877320.1
XM_017021832.1		Intron			XP_016877321.1
XM_017021833.1		Intron			XP_016877322.1
XM_017021834.1		Intron			XP_016877323.1

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