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SNP ID:
rs9927389
Gene
MIR662 MSLN
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.16: 764058 - 764058 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

CGCCAACTCCTTGGCTTCCCGTGTG[C/T]GGAGGTGTCCGGCCTGAGCACGGAG

Assay ID C__25994724_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 601051

Literature Links:

 MIR662 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.09)
(0.91)
Caucasian - Not Available CEPH (CEU)
T (0.03)
(0.97)
EAS
T (0.04)
(0.96)
African American - Not Available YRI (Yoruba)
T (0.17)
(0.83)
SAS
T (0.20)
(0.80)
Chinese - Not Available JPT (Japanese)
T (0.05)
(0.95)
AFR
T (0.14)
(0.86)
Japanese - Not Available CHB (Han Chinese)
T (0.05)
(0.95)
EUR
T (0.02)
(0.98)
AMR
T (0.04)
(0.96)
MIR662 - microRNA 662
There are no transcripts associated with this gene.
MSLN - mesothelin
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001177355.2 393 Missense Mutation GCG,GTG A,V 72 NP_001170826.1
NM_005823.5 393 Missense Mutation GCG,GTG A,V 72 NP_005814.2
NM_013404.4 393 Missense Mutation GCG,GTG A,V 72 NP_037536.2
XM_005255034.4 393 Missense Mutation GCG,GTG A,V 71 XP_005255091.1
XM_011522348.2 393 Missense Mutation GCG,GTG A,V 72 XP_011520650.1
XM_017022853.1 393 Missense Mutation GCG,GTG A,V 82 XP_016878342.1
XM_017022854.1 393 Missense Mutation GCG,GTG A,V 81 XP_016878343.1
XM_017022855.1 393 Missense Mutation GCG,GTG A,V 82 XP_016878344.1
XM_017022856.1 393 Missense Mutation GCG,GTG A,V 81 XP_016878345.1
XM_017022857.1 393 Missense Mutation GCG,GTG A,V 72 XP_016878346.1
XM_017022858.1 393 Missense Mutation GCG,GTG A,V 71 XP_016878347.1

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More Information


Set Membership:

 HapMap

Panther Classification:

Molecular Function -

cell adhesion molecule

Gene Ontology Categories:

Function(s) Process(es)


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