Product Details
- SNP ID
-
rs188096179
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:127720169 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCCAGCCTGAGAAACCATGCTTCC[A/G]TTACCGATGGTGAGTGCCCCTGCCA
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CFAP157
PubMed Links
Gene Details
- Gene
- CFAP157
- Gene Name
- cilia and flagella associated protein 157
There are no transcripts associated with this gene.
- Gene
- PTRH1
- Gene Name
- peptidyl-tRNA hydrolase 1 homolog
There are no transcripts associated with this gene.
- Gene
- TTC16
- Gene Name
- tetratricopeptide repeat domain 16
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001317037.1 |
598 |
Missense Mutation |
CAT,CGT |
H160R |
NP_001303966.1 |
NM_144965.2 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
NP_659402.1 |
XM_005251733.1 |
598 |
UTR 5 |
|
|
XP_005251790.1 |
XM_005251734.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_005251791.1 |
XM_006716970.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_006717033.1 |
XM_006716971.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_006717034.1 |
XM_011518283.1 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516585.1 |
XM_011518284.1 |
598 |
Missense Mutation |
CAT,CGT |
H125R |
XP_011516586.1 |
XM_011518285.1 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516587.1 |
XM_011518288.1 |
598 |
Missense Mutation |
CAT,CGT |
H125R |
XP_011516590.1 |
XM_011518289.2 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_011516591.1 |
XM_011518290.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_011516592.1 |
XM_011518291.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_011516593.1 |
XM_011518292.1 |
598 |
Silent Mutation |
CCA,CCG |
P3P |
XP_011516594.1 |
XM_011518293.1 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516595.1 |
XM_011518294.2 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516596.1 |
XM_011518295.1 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516597.1 |
XM_011518297.1 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516599.1 |
XM_011518298.2 |
598 |
Missense Mutation |
CAT,CGT |
H173R |
XP_011516600.1 |
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