Product Details

SNP ID
rs186075014
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:145680274 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCCTCTTACTTCTCAAGAGTTTG[A/T]TCTGATCAGACGCAAGGCTGGAGCA
Phenotype
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
C4orf51 PubMed Links

Gene Details

Gene
C4orf51
Gene Name
chromosome 4 open reading frame 51
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080531.1 172 Missense Mutation GAT,GTT D24V NP_001074000.1
XM_006714289.3 172 Missense Mutation GAT,GTT D24V XP_006714352.1
XM_011532196.2 172 Missense Mutation GAT,GTT D24V XP_011530498.1
XM_011532197.2 172 Missense Mutation GAT,GTT D24V XP_011530499.1
XM_017008547.1 172 Missense Mutation GAT,GTT D24V XP_016864036.1
XM_017008548.1 172 Missense Mutation GAT,GTT D24V XP_016864037.1
XM_017008549.1 172 Missense Mutation GAT,GTT D24V XP_016864038.1
XM_017008550.1 172 Missense Mutation GAT,GTT D24V XP_016864039.1
XM_017008551.1 172 Missense Mutation GAT,GTT D24V XP_016864040.1
XM_017008552.1 172 Missense Mutation GAT,GTT D24V XP_016864041.1
XM_017008553.1 172 Missense Mutation GAT,GTT D24V XP_016864042.1
XM_017008554.1 172 Missense Mutation GAT,GTT D24V XP_016864043.1
XM_017008555.1 172 Missense Mutation GAT,GTT D24V XP_016864044.1
XM_017008556.1 172 Missense Mutation GAT,GTT D24V XP_016864045.1

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