Product Details

SNP ID

rs143707360

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:34727304 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGCAGGTCGAGAAGATCGTTTAC[A/G]ATGTCCATTTTCCACACTTTCAGAG

Phenotype

MIM: 605299

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NCOA6 PubMed Links

Gene Details

Gene

NCOA6

Gene Name

nuclear receptor coactivator 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242539.2	6431	Missense Mutation	CGT,TGT	R1042C	NP_001229468.1
NM_001318240.1	6431	Missense Mutation	CGT,TGT	R2035C	NP_001305169.1
NM_014071.4	6431	Missense Mutation	CGT,TGT	R2035C	NP_054790.2
XM_006723755.3	6431	Intron			XP_006723818.1
XM_011528721.2	6431	Missense Mutation	CGT,TGT	R2040C	XP_011527023.1
XM_011528726.2	6431	Missense Mutation	CGT,TGT	R2029C	XP_011527028.1
XM_011528727.2	6431	Missense Mutation	CGT,TGT	R2028C	XP_011527029.1
XM_017027739.1	6431	Missense Mutation	CGT,TGT	R2059C	XP_016883228.1
XM_017027740.1	6431	Missense Mutation	CGT,TGT	R2059C	XP_016883229.1
XM_017027741.1	6431	Missense Mutation	CGT,TGT	R2058C	XP_016883230.1
XM_017027742.1	6431	Missense Mutation	CGT,TGT	R2054C	XP_016883231.1
XM_017027743.1	6431	Intron			XP_016883232.1
XM_017027744.1	6431	Missense Mutation	CGT,TGT	R2023C	XP_016883233.1
XM_017027745.1	6431	Missense Mutation	CGT,TGT	R2011C	XP_016883234.1
XM_017027746.1	6431	Intron			XP_016883235.1
XM_017027747.1	6431	Missense Mutation	CGT,TGT	R1879C	XP_016883236.1
XM_017027748.1	6431	Intron			XP_016883237.1
XM_017027749.1	6431	Intron			XP_016883238.1
XM_017027750.1	6431	Missense Mutation	CGT,TGT	R1066C	XP_016883239.1
XM_017027751.1	6431	Missense Mutation	CGT,TGT	R1042C	XP_016883240.1

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