Product Details

SNP ID
rs121912662
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7670678 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCCTTGAGTTCCAAGGCCTCATTC[G/A]GCTCTCGGAACATCTCGAAGCGCTC
Phenotype
MIM: 191170
Polymorphism
G/A, Transition Substitution
Allele Nomenclature
Literature Links
TP53 PubMed Links

Gene Details

Gene
TP53
Gene Name
tumor protein p53
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000546.5 973 Missense Mutation CCG,CTG P344L NP_000537.3
NM_001126112.2 973 Missense Mutation CCG,CTG P344L NP_001119584.1
NM_001126113.2 973 UTR 3 NP_001119585.1
NM_001126114.2 973 UTR 3 NP_001119586.1
NM_001126115.1 973 Missense Mutation CCG,CTG P212L NP_001119587.1
NM_001126116.1 973 UTR 3 NP_001119588.1
NM_001126117.1 973 UTR 3 NP_001119589.1
NM_001126118.1 973 Missense Mutation CCG,CTG P305L NP_001119590.1
NM_001276695.1 973 UTR 3 NP_001263624.1
NM_001276696.1 973 UTR 3 NP_001263625.1
NM_001276697.1 973 Missense Mutation CCG,CTG P185L NP_001263626.1
NM_001276698.1 973 UTR 3 NP_001263627.1
NM_001276699.1 973 UTR 3 NP_001263628.1
NM_001276760.1 973 Missense Mutation CCG,CTG P305L NP_001263689.1
NM_001276761.1 973 Missense Mutation CCG,CTG P305L NP_001263690.1

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