Product Details

SNP ID
rs200309674
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:192144029 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGCTATGTTGAATCTTGATTCA[C/T]AACTTTGCCTCCATTCATGGTTGGT
Phenotype
MIM: 601513
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FGF12 PubMed Links

Gene Details

Gene
FGF12
Gene Name
fibroblast growth factor 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004113.5 623 Missense Mutation ATG,GTG M176V NP_004104.3
NM_021032.4 623 Missense Mutation ATG,GTG M238V NP_066360.1
XM_005247227.2 623 Missense Mutation ATG,GTG M202V XP_005247284.1
XM_006713538.3 623 Missense Mutation ATG,GTG M173V XP_006713601.1
XM_017005879.1 623 Missense Mutation ATG,GTG M152V XP_016861368.1

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