Product Details

SNP ID

rs10157203

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:164567658 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGACAGACATAATATAAGAAGAACT[A/T]GTAATGAGAAATGACTTTTCTTTTT

Phenotype

MIM: 176310

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

PBX1 PubMed Links

Gene Details

Gene

PBX1

Gene Name

PBX homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001204961.1		Intron			NP_001191890.1
NM_001204963.1		Intron			NP_001191892.1
NM_002585.3		Intron			NP_002576.1
XM_005245228.3		Intron			XP_005245285.1
XM_005245229.3		Intron			XP_005245286.1
XM_011509590.1		Intron			XP_011507892.1
XM_011509591.2		Intron			XP_011507893.1
XM_011509592.1		Intron			XP_011507894.1
XM_017001395.1		Intron			XP_016856884.1
XM_017001396.1		Intron			XP_016856885.1

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