Product Details
- SNP ID
-
rs146022713
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:58084742 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTCGCCCTCCACGCTCTCTGGGGG[A/T]CCGCCCGCCCTAGCCCCCGCCTGGG
- Phenotype
-
- Polymorphism
- A/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ZSCAN18
PubMed Links
Gene Details
- Gene
- ZSCAN18
- Gene Name
- zinc finger and SCAN domain containing 18
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001145542.1 |
1674 |
Silent Mutation |
GGA,GGT |
G548G |
NP_001139014.1 |
| NM_001145543.1 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
NP_001139015.1 |
| NM_001145544.1 |
1674 |
Silent Mutation |
GGA,GGT |
G356G |
NP_001139016.1 |
| NM_023926.4 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
NP_076415.3 |
| XM_005259174.4 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
XP_005259231.1 |
| XM_006723335.2 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
XP_006723398.1 |
| XM_011527237.2 |
1674 |
Silent Mutation |
GGA,GGT |
G547G |
XP_011525539.1 |
| XM_011527238.1 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
XP_011525540.1 |
| XM_011527239.2 |
1674 |
Silent Mutation |
GGA,GGT |
G492G |
XP_011525541.1 |
| XM_017027169.1 |
1674 |
Silent Mutation |
GGA,GGT |
G491G |
XP_016882658.1 |
| XM_017027170.1 |
1674 |
Silent Mutation |
GGA,GGT |
G491G |
XP_016882659.1 |
| XM_017027171.1 |
1674 |
Silent Mutation |
GGA,GGT |
G491G |
XP_016882660.1 |
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