Product Details

SNP ID

rs200261536

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:48529768 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAATCTCCACCCTCCGGGCCCGGC[C/T]CAGGTACTTGTTGAAATGGAACTCC

Phenotype

MIM: 142968

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HOXB1 PubMed Links

Gene Details

Gene

HOXB1

Gene Name

homeobox B1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002144.3	691	Missense Mutation	AGC,GGC	S229G	NP_002135.2

View Full Product Details