Product Details

SNP ID: rs1060231
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:4771977 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGGCTCTCCCTCATTACCCTCTGC[C/T]TCGTCTGCATTGTGGCCAACGCCCT
Phenotype: MIM: 604657
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: TM4SF5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003963.2	86	Missense Mutation	CTC,TTC	L19F	NP_003954.2