Product Details

SNP ID
rs188952344
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48576950 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTGTAGTGAAATTCCTTCTCCAG[A/C]TCCAAGACCTGCTGGCGCGTGTAGG
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_002146.4 590 Intron NP_002137.4
XM_005257277.3 590 Intron XP_005257334.1
XM_005257280.3 590 Intron XP_005257337.1
XM_005257282.3 590 Intron XP_005257339.1
XM_006721854.2 590 Intron XP_006721917.1
XM_011524707.2 590 Intron XP_011523009.1
XM_011524708.2 590 Intron XP_011523010.1
XM_011524710.1 590 Intron XP_011523012.1
XM_011524719.1 590 Intron XP_011523021.1
XM_011524720.2 590 Intron XP_011523022.1
XM_011524721.2 590 Intron XP_011523023.1
XM_011524726.2 590 Intron XP_011523028.1
XM_017024557.1 590 Intron XP_016880046.1
XM_017024558.1 590 Intron XP_016880047.1
XM_017024559.1 590 Intron XP_016880048.1
XM_017024560.1 590 Intron XP_016880049.1
XM_017024561.1 590 Intron XP_016880050.1
XM_017024562.1 590 Intron XP_016880051.1
XM_017024563.1 590 Intron XP_016880052.1
Gene
HOXB4
Gene Name
homeobox B4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024015.4 590 Missense Mutation GAG,GAT E176D NP_076920.1
Gene
MIR10A
Gene Name
microRNA 10a
There are no transcripts associated with this gene.

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