Product Details

SNP ID
rs3177562
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:124767516 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCCAGGTCAACCCGGCCCTCTTTT[A/C]CTGGGTCCAGGGAACTTTGCTCCAT
Phenotype
MIM: 614281
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
ESAM PubMed Links

Gene Details

Gene
ESAM
Gene Name
endothelial cell adhesion molecule
There are no transcripts associated with this gene.

Gene
LOC101929340
Gene Name
uncharacterized LOC101929340
There are no transcripts associated with this gene.

Gene
MSANTD2
Gene Name
Myb/SANT DNA binding domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308027.1 2733 Missense Mutation NP_001294956.1
NM_001312919.1 2733 UTR 3 NP_001299848.1
NM_001312920.1 2733 Missense Mutation NP_001299849.1
NM_001312921.1 2733 Missense Mutation NP_001299850.1
NM_024631.3 2733 Missense Mutation NP_078907.2
XM_005271674.3 2733 Intron XP_005271731.3
XM_006718905.1 2733 Missense Mutation XP_006718968.1
XM_006718906.3 2733 Missense Mutation XP_006718969.1
XM_011542981.2 2733 UTR 3 XP_011541283.2
XM_011542982.2 2733 Intron XP_011541284.2
XM_017018295.1 2733 Missense Mutation XP_016873784.1
XM_017018296.1 2733 Missense Mutation XP_016873785.1
XM_017018297.1 2733 Missense Mutation XP_016873786.1
XM_017018298.1 2733 Missense Mutation XP_016873787.1
XM_017018299.1 2733 Intron XP_016873788.1
XM_017018300.1 2733 Intron XP_016873789.1
XM_017018301.1 2733 Intron XP_016873790.1

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