Product Details

SNP ID
rs145584999
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:19569473 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGGAGATGGTGAGGCCGCCCTT[C/T]CTGGCCAGCTCTTCTTTGGCTTCTT
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_025245.2 712 Silent Mutation AGA,AGG R248R NP_079521.1
XM_006722911.3 712 Silent Mutation AGA,AGG R162R XP_006722974.1
XM_011528320.2 712 Silent Mutation AGA,AGG R265R XP_011526622.1
XM_011528322.2 712 Silent Mutation AGA,AGG R162R XP_011526624.1
XM_017027326.1 712 Silent Mutation AGA,AGG R231R XP_016882815.1
XM_017027327.1 712 Silent Mutation AGA,AGG R217R XP_016882816.1
XM_017027328.1 712 Silent Mutation AGA,AGG R265R XP_016882817.1
XM_017027329.1 712 Silent Mutation AGA,AGG R83R XP_016882818.1
XM_017027330.1 712 Intron XP_016882819.1

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