Product Details

SNP ID
rs149526404
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:84318730 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGCTTCTTTGACATCTTTTGAGG[C/T]CTTGGTCGAATAAAGAGTACAGGGT
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 5332 UTR 3 NP_001170949.1
NM_001177479.1 5332 UTR 3 NP_001170950.1
NM_144657.4 5332 UTR 3 NP_653258.2
XM_006724619.1 5332 UTR 3 XP_006724682.1
XM_011530863.2 5332 UTR 3 XP_011529165.1
XM_011530864.1 5332 UTR 3 XP_011529166.1
XM_017029274.1 5332 UTR 3 XP_016884763.1
XM_017029275.1 5332 UTR 3 XP_016884764.1

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