Product Details

SNP ID
rs201085804
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:84321953 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACACTGAATGAGGTATCATCAGGC[A/T]CCAGTGAGGCATGATTGAAATCCAT
Phenotype
Polymorphism
A/T, Transversion 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 2109 Missense Mutation GAG,GTG E612V NP_001170949.1
NM_001177479.1 2109 Missense Mutation GAG,GTG E670V NP_001170950.1
NM_144657.4 2109 Missense Mutation GAG,GTG E670V NP_653258.2
XM_006724619.1 2109 Missense Mutation GAG,GTG E612V XP_006724682.1
XM_011530863.2 2109 Missense Mutation GAG,GTG E670V XP_011529165.1
XM_011530864.1 2109 Missense Mutation GAG,GTG E670V XP_011529166.1
XM_017029274.1 2109 Missense Mutation GAG,GTG E670V XP_016884763.1
XM_017029275.1 2109 Missense Mutation GAG,GTG E652V XP_016884764.1

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