Product Details

SNP ID

rs138198807

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:48577011 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGCTTGGGCTCCCCGCCGGCGTAA[C/T]TGGGGTTTACTGGACACACACGGAG

Phenotype

MIM: 142966 MIM: 142965 MIM: 610173

Polymorphism

C/T, Transition 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	529	Intron			NP_002137.4
XM_005257277.3	529	Intron			XP_005257334.1
XM_005257280.3	529	Intron			XP_005257337.1
XM_005257282.3	529	Intron			XP_005257339.1
XM_006721854.2	529	Intron			XP_006721917.1
XM_011524707.2	529	Intron			XP_011523009.1
XM_011524708.2	529	Intron			XP_011523010.1
XM_011524710.1	529	Intron			XP_011523012.1
XM_011524719.1	529	Intron			XP_011523021.1
XM_011524720.2	529	Intron			XP_011523022.1
XM_011524721.2	529	Intron			XP_011523023.1
XM_011524726.2	529	Intron			XP_011523028.1
XM_017024557.1	529	Intron			XP_016880046.1
XM_017024558.1	529	Intron			XP_016880047.1
XM_017024559.1	529	Intron			XP_016880048.1
XM_017024560.1	529	Intron			XP_016880049.1
XM_017024561.1	529	Intron			XP_016880050.1
XM_017024562.1	529	Intron			XP_016880051.1
XM_017024563.1	529	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	529	Missense Mutation	AAT,AGT	N156S	NP_076920.1

Gene

MIR10A

Gene Name

microRNA 10a

There are no transcripts associated with this gene.

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