Product Details

SNP ID

rs34908430

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:20784995 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTGAAGGCCGAGTGACTCAGGCC[C/T]GAGTAATCCGAGTTGTAGCCTCCGA

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	1009	Silent Mutation			NP_874359.2
NM_198956.3	1009	Silent Mutation			NP_945194.1

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