Product Details
- SNP ID
-
rs199840128
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
2
- Location
-
Chr.1:155187543 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCCAGCCTGGCACCCCAGCCCCA[C/G]ACTGGGCAGAGAAAGGAAATGGCAC
- Phenotype
-
MIM: 158340
MIM: 188062
MIM: 600986
- Polymorphism
- C/G, Transversion 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
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001018016.2 |
398 |
Missense Mutation |
TCT,TGT |
S161C |
NP_001018016.1 |
NM_001018017.2 |
398 |
Missense Mutation |
TCT,TGT |
S152C |
NP_001018017.1 |
NM_001044390.2 |
398 |
Missense Mutation |
TCT,TGT |
S100C |
NP_001037855.1 |
NM_001044391.2 |
398 |
Intron |
|
|
NP_001037856.1 |
NM_001044392.2 |
398 |
Intron |
|
|
NP_001037857.1 |
NM_001044393.2 |
398 |
Silent Mutation |
GTC,GTG |
V89V |
NP_001037858.1 |
NM_001204285.1 |
398 |
Missense Mutation |
TCT,TGT |
S372C |
NP_001191214.1 |
NM_001204286.1 |
398 |
Missense Mutation |
TCT,TGT |
S381C |
NP_001191215.1 |
NM_001204287.1 |
398 |
Missense Mutation |
TCT,TGT |
S179C |
NP_001191216.1 |
NM_001204288.1 |
398 |
Silent Mutation |
GTC,GTG |
V150V |
NP_001191217.1 |
NM_001204289.1 |
398 |
Missense Mutation |
TCT,TGT |
S135C |
NP_001191218.1 |
NM_001204290.1 |
398 |
Missense Mutation |
TCT,TGT |
S114C |
NP_001191219.1 |
NM_001204291.1 |
398 |
Missense Mutation |
TCT,TGT |
S138C |
NP_001191220.1 |
NM_001204292.1 |
398 |
Missense Mutation |
TCT,TGT |
S136C |
NP_001191221.1 |
NM_001204293.1 |
398 |
Intron |
|
|
NP_001191222.1 |
NM_001204294.1 |
398 |
Missense Mutation |
TCT,TGT |
S127C |
NP_001191223.1 |
NM_001204295.1 |
398 |
Missense Mutation |
TCT,TGT |
S86C |
NP_001191224.1 |
NM_001204296.1 |
398 |
Missense Mutation |
TCT,TGT |
S109C |
NP_001191225.1 |
NM_001204297.1 |
398 |
Intron |
|
|
NP_001191226.1 |
NM_002456.5 |
398 |
Missense Mutation |
TCT,TGT |
S170C |
NP_002447.4 |
- Gene
- THBS3
- Gene Name
- thrombospondin 3
There are no transcripts associated with this gene.
- Gene
- TRIM46
- Gene Name
- tripartite motif containing 46
There are no transcripts associated with this gene.
View Full Product Details