Product Details

SNP ID
rs12666012
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:77811731 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCTGGTACTATCTCTGTGCCAGCC[A/C]TAGCATAAGACATTTCTCTAAGCAG
Phenotype
MIM: 616785
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
PHTF2 PubMed Links

Gene Details

Gene
PHTF2
Gene Name
putative homeodomain transcription factor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127357.1 Intron NP_001120829.1
NM_001127358.1 Intron NP_001120830.1
NM_001127359.1 Intron NP_001120831.1
NM_001127360.1 Intron NP_001120832.1
NM_020432.4 Intron NP_065165.3
XM_005250508.4 Intron XP_005250565.1
XM_005250509.4 Intron XP_005250566.1
XM_006716063.3 Intron XP_006716126.1
XM_011516422.2 Intron XP_011514724.1
XM_011516423.2 Intron XP_011514725.1
XM_011516424.2 Intron XP_011514726.1
XM_017012458.1 Intron XP_016867947.1
XM_017012459.1 Intron XP_016867948.1

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