Product Details

SNP ID
rs200945027
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48578163 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCACGCCGCGCGCCGCCCGAAGC[A/C]CGCCTCCGGCTGGAAGCTGCTCTCT
Phenotype
MIM: 142966 MIM: 142965 MIM: 610173
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
HOXB3 PubMed Links

Gene Details

Gene
HOXB3
Gene Name
homeobox B3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002146.4 219 Intron NP_002137.4
XM_005257277.3 219 Intron XP_005257334.1
XM_005257280.3 219 Intron XP_005257337.1
XM_005257282.3 219 Intron XP_005257339.1
XM_006721854.2 219 Intron XP_006721917.1
XM_011524707.2 219 Intron XP_011523009.1
XM_011524708.2 219 Intron XP_011523010.1
XM_011524710.1 219 Intron XP_011523012.1
XM_011524719.1 219 Intron XP_011523021.1
XM_011524720.2 219 Intron XP_011523022.1
XM_011524721.2 219 Intron XP_011523023.1
XM_011524726.2 219 Intron XP_011523028.1
XM_017024557.1 219 Intron XP_016880046.1
XM_017024558.1 219 Intron XP_016880047.1
XM_017024559.1 219 Intron XP_016880048.1
XM_017024560.1 219 Intron XP_016880049.1
XM_017024561.1 219 Intron XP_016880050.1
XM_017024562.1 219 Intron XP_016880051.1
XM_017024563.1 219 Intron XP_016880052.1
Gene
HOXB4
Gene Name
homeobox B4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024015.4 219 Missense Mutation GGC,TGC G53C NP_076920.1
Gene
MIR10A
Gene Name
microRNA 10a
There are no transcripts associated with this gene.

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