Product Details

SNP ID: rs75182412
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:20670928 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGAGAGCTTATTCCGGGAGATCCGC[A/G]CCCAGGCCCGCGCGCTCGGGGCCGC
Phenotype: MIM: 604651
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: GDF7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182828.3	1432	Missense Mutation	ACC,GCC	T286A	NP_878248.2