Product Details

SNP ID
rs146750316
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:43387081 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTATCTGTGGTCATACATTCCGGA[A/G]AGACAGTAGCTGAGGTCTCTCCCGA
Phenotype
MIM: 601037
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HNRNPF PubMed Links

Gene Details

Gene
HNRNPF
Gene Name
heterogeneous nuclear ribonucleoprotein F
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098204.1 1212 Silent Mutation CTC,CTT L268L NP_001091674.1
NM_001098205.1 1212 Silent Mutation CTC,CTT L268L NP_001091675.1
NM_001098206.1 1212 Silent Mutation CTC,CTT L268L NP_001091676.1
NM_001098207.1 1212 Silent Mutation CTC,CTT L268L NP_001091677.1
NM_001098208.1 1212 Silent Mutation CTC,CTT L268L NP_001091678.1
NM_004966.3 1212 Silent Mutation CTC,CTT L268L NP_004957.1

View Full Product Details