Product Details

SNP ID
rs17851135
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:72968557 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAATATGAAACATGGACAGATATC[A/G]ACAAAAGAACTAGCAGATTTTGTAA
Phenotype
MIM: 613438
Polymorphism
A/G, Transition 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_001146032.1 203 Silent Mutation TCA,TCG S31S NP_001139504.1
NM_138782.2 203 Silent Mutation TCA,TCG S31S NP_620137.2
XM_017009016.1 203 Silent Mutation TCA,TCG S31S XP_016864505.1
XM_017009017.1 203 Silent Mutation TCA,TCG S31S XP_016864506.1
XM_017009018.1 203 Silent Mutation TCA,TCG S31S XP_016864507.1
XM_017009019.1 203 Silent Mutation TCA,TCG S31S XP_016864508.1
XM_017009020.1 203 Silent Mutation TCA,TCG S31S XP_016864509.1
XM_017009021.1 203 Silent Mutation TCA,TCG S31S XP_016864510.1
XM_017009022.1 203 Silent Mutation TCA,TCG S31S XP_016864511.1
XM_017009023.1 203 Silent Mutation TCA,TCG S31S XP_016864512.1

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