Product Details

SNP ID
rs142615159
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:57198765 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAACTTCCCACCTGGTTTTGAGT[A/C]AAAGCAGTTCTTGGTCTTCGGCCTC
Phenotype
MIM: 601802
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
HESX1 PubMed Links

Gene Details

Gene
HESX1
Gene Name
HESX homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003865.2 573 Missense Mutation TTG,TTT L115F NP_003856.1
XM_005265526.4 573 Missense Mutation TTG,TTT L115F XP_005265583.1
XM_006713379.3 573 Missense Mutation TTG,TTT L115F XP_006713442.1
XM_011534204.2 573 Missense Mutation TTG,TTT L115F XP_011532506.1
XM_011534205.2 573 Missense Mutation TTG,TTT L115F XP_011532507.1
XM_017007421.1 573 Missense Mutation TTG,TTT L115F XP_016862910.1

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