Product Details

SNP ID
rs137956454
Assay Type
Functionally Tested
NCBI dbSNP Submissions
3
Location
Chr.1:230906924 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGAACTAGAGTTTCTTAAGACAA[C/T]GTGGAGAAGAGTCTGTGTTTAGCAC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
TTC13 PubMed Links

Gene Details

Gene
TTC13
Gene Name
tetratricopeptide repeat domain 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001122835.2 3613 Missense Mutation CAT,CGT H801R NP_001116307.2
NM_024525.4 3613 Missense Mutation CAT,CGT H855R NP_078801.3
XM_005273260.1 3613 Missense Mutation CAT,CGT H854R XP_005273317.1
XM_005273261.2 3613 Missense Mutation CAT,CGT H824R XP_005273318.1
XM_005273262.1 3613 Missense Mutation CAT,CGT H802R XP_005273319.1
XM_005273264.2 3613 Missense Mutation CAT,CGT H779R XP_005273321.1
XM_006711814.2 3613 Missense Mutation CAT,CGT H776R XP_006711877.1
XM_006711815.2 3613 Missense Mutation CAT,CGT H497R XP_006711878.1
XM_011544275.2 3613 Missense Mutation CAT,CGT H748R XP_011542577.1
XM_011544276.2 3613 Missense Mutation CAT,CGT H558R XP_011542578.1
XM_017002321.1 3613 Missense Mutation CAT,CGT H823R XP_016857810.1
XM_017002322.1 3613 Missense Mutation CAT,CGT H778R XP_016857811.1
XM_017002323.1 3613 Missense Mutation CAT,CGT H726R XP_016857812.1
XM_017002324.1 3613 Missense Mutation CAT,CGT H725R XP_016857813.1
XM_017002325.1 3613 Missense Mutation CAT,CGT H496R XP_016857814.1
XM_017002326.1 3613 Missense Mutation CAT,CGT H496R XP_016857815.1

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