Product Details

SNP ID
rs4439802
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:49407836 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCAGCTGTTGTACTTCGCCTGATC[C/G]ATTTCTAGTTTCTTAGTCAAAGTTT
Phenotype
MIM: 176705
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
PHB PubMed Links

Gene Details

Gene
PHB
Gene Name
prohibitin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001281496.1 Intron NP_001268425.1
NM_001281497.1 Intron NP_001268426.1
NM_001281715.1 Intron NP_001268644.1
NM_002634.3 Intron NP_002625.1
XM_017024762.1 Intron XP_016880251.1
XM_017024763.1 Intron XP_016880252.1

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