Product Details

SNP ID
rs148031860
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:17843348 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAATCAGAAATGAAGATGAGACTA[C/T]CAAGACGAGCCAAAACCGCAGCACT
Phenotype
MIM: 611799 MIM: 606280
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LCORL PubMed Links

Gene Details

Gene
LCORL
Gene Name
ligand dependent nuclear receptor corepressor like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001166139.2 8185 Intron NP_001159611.1
NM_153686.8 8185 UTR 3 NP_710153.2
XM_011513821.2 8185 UTR 3 XP_011512123.1
XM_011513822.2 8185 UTR 3 XP_011512124.1
XM_011513823.2 8185 UTR 3 XP_011512125.1
XM_011513825.2 8185 Intron XP_011512127.1
XM_011513826.2 8185 UTR 3 XP_011512128.1
XM_017007961.1 8185 UTR 3 XP_016863450.1
XM_017007962.1 8185 UTR 3 XP_016863451.1
XM_017007963.1 8185 UTR 3 XP_016863452.1
XM_017007964.1 8185 Intron XP_016863453.1
XM_017007965.1 8185 Intron XP_016863454.1
Gene
NCAPG
Gene Name
non-SMC condensin I complex subunit G
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022346.4 8185 Missense Mutation CCA,TCA P991S NP_071741.2
XM_011513876.2 8185 Missense Mutation CCA,TCA P762S XP_011512178.1
XM_017008543.1 8185 Missense Mutation CCA,TCA P993S XP_016864032.1
XM_017008544.1 8185 Missense Mutation CCA,TCA P764S XP_016864033.1

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