Product Details

SNP ID
rs12314699
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:106306314 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAATACCATGTTGTCTACCTTTTT[C/G]TCAGATTCACCTATTAACATTTTGC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TCP11L2 PubMed Links

Gene Details

Gene
TCP11L2
Gene Name
t-complex 11 like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286262.1 Intron NP_001273191.1
NM_152772.2 Intron NP_689985.1
XM_005268767.4 Intron XP_005268824.1
XM_005268768.4 Intron XP_005268825.1
XM_011538129.2 Intron XP_011536431.1
XM_011538130.2 Intron XP_011536432.1
XM_011538131.2 Intron XP_011536433.1
XM_011538132.2 Intron XP_011536434.1
XM_017019127.1 Intron XP_016874616.1
XM_017019128.1 Intron XP_016874617.1
XM_017019129.1 Intron XP_016874618.1
XM_017019130.1 Intron XP_016874619.1
XM_017019131.1 Intron XP_016874620.1
XM_017019132.1 Intron XP_016874621.1
XM_017019133.1 Intron XP_016874622.1

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