Product Details

SNP ID
rs139400415
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:34727404 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTTTCAACTATCTCTTTGGGCTC[A/G]CTGCTGACAGAGGGAAGCAAAAAGT
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 6331 Silent Mutation AGC,AGT S1008S NP_001229468.1
NM_001318240.1 6331 Silent Mutation AGC,AGT S2001S NP_001305169.1
NM_014071.4 6331 Silent Mutation AGC,AGT S2001S NP_054790.2
XM_006723755.3 6331 Intron XP_006723818.1
XM_011528721.2 6331 Silent Mutation AGC,AGT S2006S XP_011527023.1
XM_011528726.2 6331 Silent Mutation AGC,AGT S1995S XP_011527028.1
XM_011528727.2 6331 Silent Mutation AGC,AGT S1994S XP_011527029.1
XM_017027739.1 6331 Silent Mutation AGC,AGT S2025S XP_016883228.1
XM_017027740.1 6331 Silent Mutation AGC,AGT S2025S XP_016883229.1
XM_017027741.1 6331 Silent Mutation AGC,AGT S2024S XP_016883230.1
XM_017027742.1 6331 Silent Mutation AGC,AGT S2020S XP_016883231.1
XM_017027743.1 6331 Intron XP_016883232.1
XM_017027744.1 6331 Silent Mutation AGC,AGT S1989S XP_016883233.1
XM_017027745.1 6331 Silent Mutation AGC,AGT S1977S XP_016883234.1
XM_017027746.1 6331 Intron XP_016883235.1
XM_017027747.1 6331 Silent Mutation AGC,AGT S1845S XP_016883236.1
XM_017027748.1 6331 Intron XP_016883237.1
XM_017027750.1 6331 Silent Mutation AGC,AGT S1032S XP_016883239.1
XM_017027751.1 6331 Silent Mutation AGC,AGT S1008S XP_016883240.1

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