Product Details

SNP ID
rs115504738
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:72993591 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATTTTTTTTTCCTCATATGAAAT[A/C]AGAATGCATTTTCAATTGATGGTAT
Phenotype
MIM: 613438
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
FCHO2 PubMed Links

Gene Details

Gene
FCHO2
Gene Name
FCH domain only 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146032.1 Intron NP_001139504.1
NM_138782.2 Intron NP_620137.2
XM_017009016.1 Intron XP_016864505.1
XM_017009017.1 Intron XP_016864506.1
XM_017009018.1 Intron XP_016864507.1
XM_017009019.1 Intron XP_016864508.1
XM_017009020.1 Intron XP_016864509.1
XM_017009021.1 Intron XP_016864510.1
XM_017009022.1 Intron XP_016864511.1
XM_017009023.1 Intron XP_016864512.1

View Full Product Details