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SNP ID: rs200177550
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:48623124 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAAGAGCGAGCGTGCAGCCAGTTGG[C/T]GGAGGGGTTGGCTGAAAGAGAAGCA
Phenotype: MIM: 142963 MIM: 142964 MIM: 608632
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: HOXB8 PubMed Links

Gene Details

Gene: HOXB8
Gene Name: homeobox B8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024016.3	733	Intron			NP_076921.1
XM_005257286.2	733	Intron			XP_005257343.1
XM_017024564.1	733	Intron			XP_016880053.1

Gene: HOXB9
Gene Name: homeobox B9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024017.4	733	Missense Mutation	ACC,GCC	T177A	NP_076922.1

Gene: MIR196A1
Gene Name: microRNA 196a-1

There are no transcripts associated with this gene.

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