Product Details

SNP ID

rs5922966

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:84336858 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTCCTTATGAGCCCTTGCATCATT[C/T]GGAACAACTTCATTGGGCTCTTCTA

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	1783	Silent Mutation	CCA,CCG	P503P	NP_001170949.1
NM_001177479.1	1783	Silent Mutation	CCA,CCG	P561P	NP_001170950.1
NM_144657.4	1783	Silent Mutation	CCA,CCG	P561P	NP_653258.2
XM_006724619.1	1783	Silent Mutation	CCA,CCG	P503P	XP_006724682.1
XM_011530863.2	1783	Silent Mutation	CCA,CCG	P561P	XP_011529165.1
XM_011530864.1	1783	Silent Mutation	CCA,CCG	P561P	XP_011529166.1
XM_017029274.1	1783	Silent Mutation	CCA,CCG	P561P	XP_016884763.1
XM_017029275.1	1783	Silent Mutation	CCA,CCG	P543P	XP_016884764.1

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