Product Details

SNP ID
rs9676775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:19564435 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTTCCAAGTCTTTGCTATTGTGAA[C/T]TGTATTTTTAGTGGAGATGGGGTTT
Phenotype
MIM: 608127
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PBX4 PubMed Links

Gene Details

Gene
PBX4
Gene Name
PBX homeobox 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025245.2 Intron NP_079521.1
XM_006722911.3 Intron XP_006722974.1
XM_011528320.2 Intron XP_011526622.1
XM_011528322.2 Intron XP_011526624.1
XM_017027326.1 Intron XP_016882815.1
XM_017027327.1 Intron XP_016882816.1
XM_017027328.1 Intron XP_016882817.1
XM_017027329.1 Intron XP_016882818.1
XM_017027330.1 Intron XP_016882819.1

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