Product Details

SNP ID

rs11039155

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47259211 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCTTGGTAATGACCAGGGCTCCAG[A/G]AAGAGATGTCCTTGTGGCTGGGGGC

Phenotype

MIM: 602423

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

NR1H3 PubMed Links

Gene Details

Gene

NR1H3

Gene Name

nuclear receptor subfamily 1 group H member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130101.2	198	UTR 5			NP_001123573.1
NM_001130102.2	198	Intron			NP_001123574.1
NM_001251934.1	198	Intron			NP_001238863.1
NM_001251935.1	198	Intron			NP_001238864.1
NM_005693.3	198	UTR 5			NP_005684.2
XM_005252705.1	198	UTR 5			XP_005252762.1
XM_005252706.1	198	UTR 5			XP_005252763.1
XM_005252707.4	198	UTR 5			XP_005252764.1
XM_005252709.1	198	UTR 5			XP_005252766.1
XM_005252710.1	198	UTR 5			XP_005252767.1
XM_005252713.3	198	UTR 5			XP_005252770.1
XM_005252715.2	198	UTR 5			XP_005252772.1
XM_005252716.3	198	Intron			XP_005252773.1
XM_005252718.3	198	Intron			XP_005252775.1
XM_006718112.1	198	UTR 5			XP_006718175.1
XM_006718113.1	198	UTR 5			XP_006718176.1
XM_006718115.1	198	UTR 5			XP_006718178.1
XM_006718116.1	198	Intron			XP_006718179.1
XM_011519805.2	198	UTR 5			XP_011518107.1
XM_011519806.1	198	Intron			XP_011518108.1
XM_011519807.1	198	Intron			XP_011518109.1
XM_011519808.2	198	Intron			XP_011518110.1
XM_017017056.1	198	Intron			XP_016872545.1
XM_017017057.1	198	Intron			XP_016872546.1
XM_017017058.1	198	Intron			XP_016872547.1

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