Product Details

SNP ID
rs143487849
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:84326256 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAGTCTGAAGTTTAAAGTATTTTTG[C/T]TTTTGAATCTCGAGCTCATTTTCAA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HDX PubMed Links

Gene Details

Gene
HDX
Gene Name
highly divergent homeobox
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177478.1 1969 Silent Mutation AAA,AAG K565K NP_001170949.1
NM_001177479.1 1969 Silent Mutation AAA,AAG K623K NP_001170950.1
NM_144657.4 1969 Silent Mutation AAA,AAG K623K NP_653258.2
XM_006724619.1 1969 Silent Mutation AAA,AAG K565K XP_006724682.1
XM_011530863.2 1969 Silent Mutation AAA,AAG K623K XP_011529165.1
XM_011530864.1 1969 Silent Mutation AAA,AAG K623K XP_011529166.1
XM_017029274.1 1969 Silent Mutation AAA,AAG K623K XP_016884763.1
XM_017029275.1 1969 Silent Mutation AAA,AAG K605K XP_016884764.1

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