Product Details

SNP ID
rs148853182
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:89737620 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCTGTGTGCCTTATGGATGTGGC[A/C]AAGCGTGAAATCATCTGTGCCTTTG
Phenotype
MIM: 608689
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
MESP1 PubMed Links

Gene Details

Gene
MESP1
Gene Name
mesoderm posterior bHLH transcription factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018670.3 1679 Intron NP_061140.1
Gene
WDR93
Gene Name
WD repeat domain 93
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001284395.1 1679 Silent Mutation GCA,GCC A524A NP_001271324.1
NM_001284396.1 1679 Intron NP_001271325.1
NM_020212.1 1679 Silent Mutation GCA,GCC A552A NP_064597.1
XM_006720614.1 1679 Missense Mutation CAA,CCA Q531P XP_006720677.1
XM_006720615.1 1679 Missense Mutation CAA,CCA Q502P XP_006720678.1
XM_006720618.2 1679 Intron XP_006720681.1
XM_011521794.2 1679 Missense Mutation CAA,CCA Q531P XP_011520096.1
XM_011521795.1 1679 Missense Mutation CAA,CCA Q531P XP_011520097.1
XM_011521796.2 1679 Missense Mutation CAA,CCA Q531P XP_011520098.1
XM_011521798.2 1679 Missense Mutation CAA,CCA Q333P XP_011520100.1
XM_011521800.1 1679 Missense Mutation CAA,CCA Q333P XP_011520102.1
XM_011521802.2 1679 Intron XP_011520104.1
XM_017022415.1 1679 Missense Mutation CAA,CCA Q355P XP_016877904.1
XM_017022416.1 1679 Missense Mutation CAA,CCA Q333P XP_016877905.1
XM_017022417.1 1679 Intron XP_016877906.1

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