Product Details

SNP ID
rs112273344
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:33043933 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCCCCAAAGAGTGCAGAGACCT[A/C]ACTGTAAGCAAATTTGACTTTGGTT
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
TCP11L1 PubMed Links

Gene Details

Gene
TCP11L1
Gene Name
t-complex 11 like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145541.1 559 Missense Mutation AAC,CAC N54H NP_001139013.1
NM_018393.3 559 Missense Mutation AAC,CAC N54H NP_060863.3
XM_011520204.2 559 Missense Mutation AAC,CAC N54H XP_011518506.1
XM_011520205.2 559 Missense Mutation AAC,CAC N54H XP_011518507.1
XM_011520206.2 559 Missense Mutation AAC,CAC N54H XP_011518508.1
XM_011520207.2 559 Missense Mutation AAC,CAC N54H XP_011518509.1
XM_017017989.1 559 Missense Mutation AAC,CAC N54H XP_016873478.1
XM_017017990.1 559 Missense Mutation AAC,CAC N54H XP_016873479.1
XM_017017991.1 559 UTR 5 XP_016873480.1
XM_017017992.1 559 Intron XP_016873481.1

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