Product Details

SNP ID
rs148455331
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:53940391 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGAGGAGGAGGTGACAAGTTGTGG[C/T]GTGGCAGCCACAGTGGGGGCTGGTA
Phenotype
MIM: 300560
Polymorphism
C/T, Transition 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 3578 Silent Mutation ACA,ACG T961T NP_001171825.1
NM_001184897.1 3578 Silent Mutation ACA,ACG T824T NP_001171826.1
NM_001184898.1 3578 Intron NP_001171827.1
NM_015107.2 3578 Silent Mutation ACA,ACG T925T NP_055922.1
XM_005261996.1 3578 Silent Mutation ACA,ACG T961T XP_005262053.1
XM_005261997.3 3578 Silent Mutation ACA,ACG T925T XP_005262054.1
XM_005261999.1 3578 Silent Mutation ACA,ACG T925T XP_005262056.1
XM_005262000.1 3578 Silent Mutation ACA,ACG T860T XP_005262057.1
XM_011530778.1 3578 Silent Mutation ACA,ACG T961T XP_011529080.1
XM_017029361.1 3578 Silent Mutation ACA,ACG T925T XP_016884850.1
XM_017029362.1 3578 Silent Mutation ACA,ACG T925T XP_016884851.1

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