Product Details

SNP ID
rs199745484
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:23534435 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTAGACACGCTTGAGTGCTCCGA[A/G]GGCAGGTGAGGGGAGGGCATCCCAG
Phenotype
MIM: 604975
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SOX5 PubMed Links

Gene Details

Gene
SOX5
Gene Name
SRY-box 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261414.1 2223 Silent Mutation CCC,CCT P571P NP_001248343.1
NM_001261415.1 2223 Silent Mutation CCC,CCT P682P NP_001248344.1
NM_006940.4 2223 Silent Mutation CCC,CCT P692P NP_008871.3
NM_152989.3 2223 Silent Mutation CCC,CCT P679P NP_694534.1
NM_178010.2 2223 Silent Mutation CCC,CCT P306P NP_821078.1
XM_011520831.2 2223 Silent Mutation CCC,CCT P657P XP_011519133.1
XM_011520832.2 2223 Silent Mutation CCC,CCT P693P XP_011519134.1
XM_011520833.2 2223 Silent Mutation CCC,CCT P683P XP_011519135.1
XM_011520834.2 2223 Silent Mutation CCC,CCT P680P XP_011519136.1
XM_011520835.2 2223 Silent Mutation CCC,CCT P680P XP_011519137.1
XM_011520837.2 2223 Silent Mutation CCC,CCT P680P XP_011519139.1
XM_011520838.2 2223 Silent Mutation CCC,CCT P658P XP_011519140.1
XM_011520842.2 2223 Silent Mutation CCC,CCT P344P XP_011519144.1
XM_017019888.1 2223 Silent Mutation CCC,CCT P722P XP_016875377.1
XM_017019889.1 2223 Silent Mutation CCC,CCT P721P XP_016875378.1
XM_017019890.1 2223 Silent Mutation CCC,CCT P680P XP_016875379.1
XM_017019891.1 2223 Silent Mutation CCC,CCT P680P XP_016875380.1
XM_017019892.1 2223 Silent Mutation CCC,CCT P680P XP_016875381.1
XM_017019893.1 2223 Silent Mutation CCC,CCT P680P XP_016875382.1
XM_017019894.1 2223 Silent Mutation CCC,CCT P680P XP_016875383.1
XM_017019895.1 2223 Silent Mutation CCC,CCT P680P XP_016875384.1
XM_017019896.1 2223 Silent Mutation CCC,CCT P679P XP_016875385.1
XM_017019897.1 2223 Silent Mutation CCC,CCT P645P XP_016875386.1
XM_017019898.1 2223 Silent Mutation CCC,CCT P644P XP_016875387.1
XM_017019899.1 2223 Silent Mutation CCC,CCT P644P XP_016875388.1
XM_017019900.1 2223 Silent Mutation CCC,CCT P644P XP_016875389.1
XM_017019901.1 2223 Silent Mutation CCC,CCT P644P XP_016875390.1
XM_017019902.1 2223 Intron XP_016875391.1
XM_017019903.1 2223 Intron XP_016875392.1

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