Product Details

SNP ID
rs141494832
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:8915842 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCTTTACATTTTTATTTCTAGTT[C/G]ACAATCCAAAAAAAATTATTAATCA
Phenotype
MIM: 602978
Polymorphism
C/G, 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_004426.2 225 Intron NP_004417.2
XM_005253334.2 225 Intron XP_005253391.1
XM_011520599.2 225 Intron XP_011518901.1
XM_011520600.2 225 Intron XP_011518902.1
XM_011520603.2 225 Intron XP_011518905.1
XM_017018955.1 225 UTR 5 XP_016874444.1
XM_017018956.1 225 Intron XP_016874445.1
XM_017018957.1 225 Intron XP_016874446.1
XM_017018958.1 225 Intron XP_016874447.1

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