Product Details
- SNP ID
-
rs146863606
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:52116390 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TATGAGTTTGTTCTCCTCCTCTATC[A/G]TCTTTAAGTTGCTCTCCATAGATGT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ST18
PubMed Links
Gene Details
- Gene
- ST18
- Gene Name
- ST18, C2H2C-type zinc finger
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014682.2 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
NP_055497.1 |
XM_006716487.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_006716550.1 |
XM_011517629.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515931.1 |
XM_011517631.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515933.1 |
XM_011517632.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515934.1 |
XM_011517633.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515935.1 |
XM_011517634.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515936.1 |
XM_011517635.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515937.1 |
XM_011517636.2 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515938.1 |
XM_011517637.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515939.1 |
XM_011517638.2 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_011515940.1 |
XM_011517641.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_011515943.1 |
XM_011517642.1 |
3417 |
Missense Mutation |
ACG,ATG |
T881M |
XP_011515944.1 |
XM_017014047.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869536.1 |
XM_017014048.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869537.1 |
XM_017014049.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869538.1 |
XM_017014050.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869539.1 |
XM_017014051.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869540.1 |
XM_017014052.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869541.1 |
XM_017014053.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869542.1 |
XM_017014054.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869543.1 |
XM_017014055.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869544.1 |
XM_017014056.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869545.1 |
XM_017014057.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869546.1 |
XM_017014058.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869547.1 |
XM_017014059.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869548.1 |
XM_017014060.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869549.1 |
XM_017014061.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869550.1 |
XM_017014062.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869551.1 |
XM_017014063.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869552.1 |
XM_017014064.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869553.1 |
XM_017014065.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869554.1 |
XM_017014066.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869555.1 |
XM_017014067.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869556.1 |
XM_017014068.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869557.1 |
XM_017014069.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869558.1 |
XM_017014070.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869559.1 |
XM_017014071.1 |
3417 |
Missense Mutation |
ACG,ATG |
T963M |
XP_016869560.1 |
XM_017014072.1 |
3417 |
Missense Mutation |
ACG,ATG |
T934M |
XP_016869561.1 |
XM_017014073.1 |
3417 |
Missense Mutation |
ACG,ATG |
T934M |
XP_016869562.1 |
XM_017014074.1 |
3417 |
Missense Mutation |
ACG,ATG |
T934M |
XP_016869563.1 |
XM_017014075.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869564.1 |
XM_017014076.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869565.1 |
XM_017014077.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869566.1 |
XM_017014078.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869567.1 |
XM_017014079.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869568.1 |
XM_017014080.1 |
3417 |
Missense Mutation |
ACG,ATG |
T928M |
XP_016869569.1 |
XM_017014081.1 |
3417 |
Missense Mutation |
ACG,ATG |
T881M |
XP_016869570.1 |
XM_017014082.1 |
3417 |
Missense Mutation |
ACG,ATG |
T881M |
XP_016869571.1 |
XM_017014083.1 |
3417 |
Missense Mutation |
ACG,ATG |
T881M |
XP_016869572.1 |
XM_017014084.1 |
3417 |
Missense Mutation |
ACG,ATG |
T881M |
XP_016869573.1 |
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