Product Details

SNP ID

rs145875827

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:20785652 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTTGCAGCTGGCGGAAGAAGAGGA[C/T]GAGGAGCGTTTCCAGGGGTGGAAGC

Phenotype

MIM: 608306

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SP8 PubMed Links

Gene Details

Gene

SP8

Gene Name

Sp8 transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182700.5	352	Silent Mutation	TCA,TCG	S55S	NP_874359.2
NM_198956.3	352	Silent Mutation	TCA,TCG	S37S	NP_945194.1

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