Product Details

SNP ID

rs13392217

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:173909983 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCAGAAACTGTGACAAGCTGTAA[A/G]GGTATTTCAGTGTTGGTAAGGATAT

Phenotype

MIM: 601804

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SP3 PubMed Links

Gene Details

Gene

SP3

Gene Name

Sp3 transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017371.4	2826	Silent Mutation	CCC,CCT	P700P	NP_001017371.3
NM_001172712.1	2826	Silent Mutation	CCC,CCT	P765P	NP_001166183.1
NM_003111.4	2826	Silent Mutation	CCC,CCT	P768P	NP_003102.1

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