Product Details
- SNP ID
-
rs145036285
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:85695275 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAAGTATTGGGGGAGTTTACCATCT[C/T]CTCCCAGAGAGCAACTTCCTCTGAA
- Phenotype
-
MIM: 612880
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CCDC89
PubMed Links
Gene Details
- Gene
- CCDC89
- Gene Name
- coiled-coil domain containing 89
There are no transcripts associated with this gene.
- Gene
- SYTL2
- Gene Name
- synaptotagmin like 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001162951.2 |
6708 |
Missense Mutation |
AAG,GAG |
K909E |
NP_001156423.1 |
NM_001162952.2 |
6708 |
Missense Mutation |
AAG,GAG |
K311E |
NP_001156424.1 |
NM_001162953.2 |
6708 |
Missense Mutation |
AAG,GAG |
K910E |
NP_001156425.1 |
NM_001289608.1 |
6708 |
Missense Mutation |
AAG,GAG |
K877E |
NP_001276537.1 |
NM_001289609.1 |
6708 |
Missense Mutation |
AAG,GAG |
K230E |
NP_001276538.1 |
NM_001289610.1 |
6708 |
Missense Mutation |
AAG,GAG |
K311E |
NP_001276539.1 |
NM_032943.4 |
6708 |
Missense Mutation |
AAG,GAG |
K885E |
NP_116561.1 |
NM_206929.3 |
6708 |
Missense Mutation |
AAG,GAG |
K351E |
NP_996812.1 |
NM_206930.3 |
6708 |
Missense Mutation |
AAG,GAG |
K340E |
NP_996813.1 |
XM_005274057.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2198E |
XP_005274114.1 |
XM_005274060.1 |
6708 |
Missense Mutation |
AAG,GAG |
K926E |
XP_005274117.1 |
XM_005274061.1 |
6708 |
Missense Mutation |
AAG,GAG |
K925E |
XP_005274118.1 |
XM_005274062.2 |
6708 |
Missense Mutation |
AAG,GAG |
K899E |
XP_005274119.1 |
XM_005274063.1 |
6708 |
Missense Mutation |
AAG,GAG |
K886E |
XP_005274120.1 |
XM_005274066.1 |
6708 |
Missense Mutation |
AAG,GAG |
K869E |
XP_005274123.1 |
XM_005274067.4 |
6708 |
Missense Mutation |
AAG,GAG |
K351E |
XP_005274124.1 |
XM_011545105.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2214E |
XP_011543407.1 |
XM_011545106.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2213E |
XP_011543408.1 |
XM_011545107.2 |
6708 |
Missense Mutation |
AAG,GAG |
K2187E |
XP_011543409.1 |
XM_011545108.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2174E |
XP_011543410.1 |
XM_011545109.2 |
6708 |
Missense Mutation |
AAG,GAG |
K2165E |
XP_011543411.1 |
XM_011545110.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2157E |
XP_011543412.1 |
XM_011545112.1 |
6708 |
Intron |
|
|
XP_011543414.1 |
XM_011545114.2 |
6708 |
Missense Mutation |
AAG,GAG |
K340E |
XP_011543416.1 |
XM_011545115.1 |
6708 |
Missense Mutation |
AAG,GAG |
K300E |
XP_011543417.1 |
XM_011545116.2 |
6708 |
Missense Mutation |
AAG,GAG |
K300E |
XP_011543418.1 |
XM_017017933.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2197E |
XP_016873422.1 |
XM_017017934.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2186E |
XP_016873423.1 |
XM_017017935.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2146E |
XP_016873424.1 |
XM_017017936.1 |
6708 |
Missense Mutation |
AAG,GAG |
K2071E |
XP_016873425.1 |
XM_017017937.1 |
6708 |
Missense Mutation |
AAG,GAG |
K851E |
XP_016873426.1 |
XM_017017938.1 |
6708 |
Missense Mutation |
AAG,GAG |
K837E |
XP_016873427.1 |
XM_017017939.1 |
6708 |
Missense Mutation |
AAG,GAG |
K420E |
XP_016873428.1 |
XM_017017940.1 |
6708 |
Missense Mutation |
AAG,GAG |
K404E |
XP_016873429.1 |
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