Product Details
- SNP ID
-
rs143725166
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:85697988 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCATCAATACTATTACCATTTAACA[A/G]AAGAATTTAGATGACTTCCCCTTAG
- Phenotype
-
MIM: 612880
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SYTL2
PubMed Links
Gene Details
- Gene
- SYTL2
- Gene Name
- synaptotagmin like 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001162951.2 |
6427 |
Missense Mutation |
TCT,TTT |
S815F |
NP_001156423.1 |
NM_001162952.2 |
6427 |
Missense Mutation |
TCT,TTT |
S217F |
NP_001156424.1 |
NM_001162953.2 |
6427 |
Missense Mutation |
TCT,TTT |
S816F |
NP_001156425.1 |
NM_001289608.1 |
6427 |
Missense Mutation |
TCT,TTT |
S783F |
NP_001276537.1 |
NM_001289609.1 |
6427 |
Missense Mutation |
TCT,TTT |
S136F |
NP_001276538.1 |
NM_001289610.1 |
6427 |
Missense Mutation |
TCT,TTT |
S217F |
NP_001276539.1 |
NM_032943.4 |
6427 |
Missense Mutation |
TCT,TTT |
S791F |
NP_116561.1 |
NM_206929.3 |
6427 |
Missense Mutation |
TCT,TTT |
S257F |
NP_996812.1 |
NM_206930.3 |
6427 |
Missense Mutation |
TCT,TTT |
S246F |
NP_996813.1 |
XM_005274057.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2104F |
XP_005274114.1 |
XM_005274060.1 |
6427 |
Missense Mutation |
TCT,TTT |
S832F |
XP_005274117.1 |
XM_005274061.1 |
6427 |
Missense Mutation |
TCT,TTT |
S831F |
XP_005274118.1 |
XM_005274062.2 |
6427 |
Missense Mutation |
TCT,TTT |
S805F |
XP_005274119.1 |
XM_005274063.1 |
6427 |
Missense Mutation |
TCT,TTT |
S792F |
XP_005274120.1 |
XM_005274066.1 |
6427 |
Missense Mutation |
TCT,TTT |
S775F |
XP_005274123.1 |
XM_005274067.4 |
6427 |
Missense Mutation |
TCT,TTT |
S257F |
XP_005274124.1 |
XM_011545105.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2120F |
XP_011543407.1 |
XM_011545106.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2119F |
XP_011543408.1 |
XM_011545107.2 |
6427 |
Missense Mutation |
TCT,TTT |
S2093F |
XP_011543409.1 |
XM_011545108.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2080F |
XP_011543410.1 |
XM_011545109.2 |
6427 |
Missense Mutation |
TCT,TTT |
S2071F |
XP_011543411.1 |
XM_011545110.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2063F |
XP_011543412.1 |
XM_011545112.1 |
6427 |
Intron |
|
|
XP_011543414.1 |
XM_011545114.2 |
6427 |
Missense Mutation |
TCT,TTT |
S246F |
XP_011543416.1 |
XM_011545115.1 |
6427 |
Missense Mutation |
TCT,TTT |
S206F |
XP_011543417.1 |
XM_011545116.2 |
6427 |
Missense Mutation |
TCT,TTT |
S206F |
XP_011543418.1 |
XM_017017933.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2103F |
XP_016873422.1 |
XM_017017934.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2092F |
XP_016873423.1 |
XM_017017935.1 |
6427 |
Missense Mutation |
TCT,TTT |
S2052F |
XP_016873424.1 |
XM_017017936.1 |
6427 |
Missense Mutation |
TCT,TTT |
S1977F |
XP_016873425.1 |
XM_017017937.1 |
6427 |
Missense Mutation |
TCT,TTT |
S757F |
XP_016873426.1 |
XM_017017938.1 |
6427 |
Missense Mutation |
TCT,TTT |
S743F |
XP_016873427.1 |
XM_017017939.1 |
6427 |
Missense Mutation |
TCT,TTT |
S326F |
XP_016873428.1 |
XM_017017940.1 |
6427 |
Missense Mutation |
TCT,TTT |
S310F |
XP_016873429.1 |
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