Product Details

SNP ID
rs201150017
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:8919860 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCAGCTGCATAGCCTGGCTGCCGT[A/C]CAGCAGGTGAGAGGTCAGCAGCCAG
Phenotype
MIM: 602978
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
PHC1 PubMed Links

Gene Details

Gene
PHC1
Gene Name
polyhomeotic homolog 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004426.2 719 Intron NP_004417.2
XM_005253334.2 719 Intron XP_005253391.1
XM_011520599.2 719 Intron XP_011518901.1
XM_011520600.2 719 Intron XP_011518902.1
XM_011520603.2 719 Intron XP_011518905.1
XM_017018955.1 719 Silent Mutation GTA,GTC V73V XP_016874444.1
XM_017018956.1 719 Intron XP_016874445.1
XM_017018957.1 719 Intron XP_016874446.1
XM_017018958.1 719 Intron XP_016874447.1

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