Product Details

SNP ID
rs116197244
Assay Type
Functionally Tested
NCBI dbSNP Submissions
10
Location
Chr.1:18632669 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTTTTTTTTAAATTACTCTTCCT[A/G]TGATCGTTTGAGTCCCTGGCGCGTG
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 Intron NP_001128726.1
NM_002584.2 Intron NP_002575.1
NM_013945.2 Intron NP_039236.1

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