Product Details

SNP ID

rs141499812

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:18635119 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACCTCCACCTCTGAAGCAGGTGGC[A/G]ACTCCGGATGTAGAGAAAAAGATTG

Phenotype

MIM: 167410

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PAX7 PubMed Links

Gene Details

Gene

PAX7

Gene Name

paired box 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135254.1	928	Silent Mutation	GCA,GCG	A110A	NP_001128726.1
NM_002584.2	928	Silent Mutation	GCA,GCG	A110A	NP_002575.1
NM_013945.2	928	Silent Mutation	GCA,GCG	A110A	NP_039236.1

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