Product Details

SNP ID
rs1794296
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:7686283 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCATCATTGCACTCTTTCAAAATTT[C/G]ATTCTCAGACGTACCCATTCTTTTT
Phenotype
MIM: 191170 MIM: 612661
Polymorphism
C/G, Transversion 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 Intron NP_000537.3
NM_001126112.2 Intron NP_001119584.1
NM_001126113.2 Intron NP_001119585.1
NM_001126114.2 Intron NP_001119586.1
NM_001126115.1 Intron NP_001119587.1
NM_001126116.1 Intron NP_001119588.1
NM_001126117.1 Intron NP_001119589.1
NM_001126118.1 Intron NP_001119590.1
NM_001276695.1 Intron NP_001263624.1
NM_001276696.1 Intron NP_001263625.1
NM_001276697.1 Intron NP_001263626.1
NM_001276698.1 Intron NP_001263627.1
NM_001276699.1 Intron NP_001263628.1
NM_001276760.1 Intron NP_001263689.1
NM_001276761.1 Intron NP_001263690.1
Gene
WRAP53
Gene Name
WD repeat containing antisense to TP53
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143990.1 Intron NP_001137462.1
NM_001143991.1 Intron NP_001137463.1
NM_001143992.1 Intron NP_001137464.1
NM_018081.2 Intron NP_060551.2
XM_011523952.2 Intron XP_011522254.1
XM_017024812.1 Intron XP_016880301.1

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