Product Details

SNP ID
rs8017662
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:104696224 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGGGGGCCCTCTTTGCACAACAAG[C/T]GGAGTTCAAGATCTTGGAGGGCTTT
Phenotype
MIM: 610982
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
INF2 PubMed Links

Gene Details

Gene
INF2
Gene Name
inverted formin, FH2 and WH2 domain containing
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031714.3 Intron NP_001026884.3
NM_022489.3 Intron NP_071934.3
NM_032714.2 Intron NP_116103.1
XM_005268004.4 Intron XP_005268061.1
XM_005268005.4 Intron XP_005268062.1
XM_017021595.1 Intron XP_016877084.1

View Full Product Details