Product Details

SNP ID
rs140640141
Assay Type
Functionally tested
NCBI dbSNP Submissions
6
Location
Chr.1:155197916 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGGGTCACTGTTCATGGTCTGAA[C/T]GATTTCCATGCCCTGGGGTTGTATA
Phenotype
MIM: 158340 MIM: 188062
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MIR92B PubMed Links

Gene Details

Gene
MIR92B
Gene Name
microRNA 92b
There are no transcripts associated with this gene.

Gene
MUC1
Gene Name
mucin 1, cell surface associated
There are no transcripts associated with this gene.

Gene
THBS3
Gene Name
thrombospondin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252607.1 2322 Missense Mutation NP_001239536.1
NM_001252608.1 2322 Missense Mutation NP_001239537.1
NM_007112.4 2322 Missense Mutation NP_009043.1
XM_006711498.3 2322 Missense Mutation XP_006711561.1
XM_011509926.2 2322 Missense Mutation XP_011508228.1
XM_011509927.2 2322 Missense Mutation XP_011508229.1
XM_011509928.2 2322 Missense Mutation XP_011508230.1
XM_011509929.1 2322 Missense Mutation XP_011508231.1
XM_011509930.2 2322 Missense Mutation XP_011508232.1
XM_011509931.1 2322 Missense Mutation XP_011508233.1
XM_011509932.2 2322 Missense Mutation XP_011508234.1
XM_011509933.1 2322 Missense Mutation XP_011508235.1
XM_011509934.1 2322 Missense Mutation XP_011508236.1
XM_011509935.1 2322 Missense Mutation XP_011508237.1
XM_011509936.1 2322 Missense Mutation XP_011508238.1
XM_017002206.1 2322 Missense Mutation XP_016857695.1

View Full Product Details