Product Details

SNP ID
rs7876951
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:53946916 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTTTCAAGCAAAGAAAAAAATTT[A/T]AAAAACAAGATAGTGATAAATGAAG
Phenotype
MIM: 300560
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
PHF8 PubMed Links

Gene Details

Gene
PHF8
Gene Name
PHD finger protein 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184896.1 Intron NP_001171825.1
NM_001184897.1 Intron NP_001171826.1
NM_001184898.1 Intron NP_001171827.1
NM_015107.2 Intron NP_055922.1
XM_005261996.1 Intron XP_005262053.1
XM_005261997.3 Intron XP_005262054.1
XM_005261999.1 Intron XP_005262056.1
XM_005262000.1 Intron XP_005262057.1
XM_011530778.1 Intron XP_011529080.1
XM_017029361.1 Intron XP_016884850.1
XM_017029362.1 Intron XP_016884851.1

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