Product Details

SNP ID
rs188050043
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:118194335 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACTCTCCATTCTTCTCAAAAGGCT[C/T]GCTGTGTTTTTGGCATTCCCCCACC
Phenotype
MIM: 609770
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
JAML PubMed Links

Gene Details

Gene
JAML
Gene Name
junction adhesion molecule like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098526.1 1287 Missense Mutation NP_001091996.1
NM_001286570.1 1287 Missense Mutation NP_001273499.1
NM_001286571.1 1287 Missense Mutation NP_001273500.1
NM_153206.2 1287 Missense Mutation NP_694938.2
XM_005271407.3 1287 Missense Mutation XP_005271464.1
XM_017017213.1 1287 Missense Mutation XP_016872702.1
XM_017017214.1 1287 Missense Mutation XP_016872703.1
XM_017017215.1 1287 Missense Mutation XP_016872704.1

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