Product Details

SNP ID

rs1421314

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:7688222 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGGGCGGTGCAGGTGCTTTAAGAAT[C/T]ACCGCGGGACTCGGTAGGGGGAGCG

Phenotype

MIM: 191170 MIM: 612661

Polymorphism

C/T, 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	651	Intron			NP_000537.3
NM_001126112.2	651	Intron			NP_001119584.1
NM_001126113.2	651	Intron			NP_001119585.1
NM_001126114.2	651	Intron			NP_001119586.1
NM_001126115.1	651	Intron			NP_001119587.1
NM_001126116.1	651	Intron			NP_001119588.1
NM_001126117.1	651	Intron			NP_001119589.1
NM_001126118.1	651	Intron			NP_001119590.1
NM_001276695.1	651	Intron			NP_001263624.1
NM_001276696.1	651	Intron			NP_001263625.1
NM_001276697.1	651	Intron			NP_001263626.1
NM_001276698.1	651	Intron			NP_001263627.1
NM_001276699.1	651	Intron			NP_001263628.1
NM_001276760.1	651	Intron			NP_001263689.1
NM_001276761.1	651	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	651	Intron			NP_001137462.1
NM_001143991.1	651	Intron			NP_001137463.1
NM_001143992.1	651	Intron			NP_001137464.1
NM_018081.2	651	Intron			NP_060551.2
XM_011523952.2	651	Intron			XP_011522254.1
XM_017024812.1	651	UTR 5			XP_016880301.1

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