Product Details

SNP ID
rs190025961
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:192144076 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGTGTTCCAGAACTTTTCCTTGAA[C/T]GCCCTTGTTTTTCTCCAATTTCATG
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_004113.5 576 Missense Mutation CAT,CGT H160R NP_004104.3
NM_021032.4 576 Missense Mutation CAT,CGT H222R NP_066360.1
XM_005247227.2 576 Missense Mutation CAT,CGT H186R XP_005247284.1
XM_006713538.3 576 Missense Mutation CAT,CGT H157R XP_006713601.1
XM_017005879.1 576 Missense Mutation CAT,CGT H136R XP_016861368.1

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