Product Details

SNP ID
rs6622999
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:84332580 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTGACATATTTGAGAGTGCTAAGA[A/G]GAGCACTCTTAACAGCTGTGCAATC
Phenotype
Polymorphism
A/G, 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 Intron NP_001170949.1
NM_001177479.1 Intron NP_001170950.1
NM_144657.4 Intron NP_653258.2
XM_006724619.1 Intron XP_006724682.1
XM_011530863.2 Intron XP_011529165.1
XM_011530864.1 Intron XP_011529166.1
XM_017029274.1 Intron XP_016884763.1
XM_017029275.1 Intron XP_016884764.1

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