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Search Thermo Fisher Scientific
TCCAAGTATTGGGGGAGTTTACCAT[A/C]TTCTCCCAGAGAGCAACTTCCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612880 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC89 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
CCDC89 - coiled-coil domain containing 89 | ||||||
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There are no transcripts associated with this gene. |
SYTL2 - synaptotagmin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001162951.2 | 6710 | Missense Mutation | AAG,AAT | K,N 909 | NP_001156423.1 | |
NM_001162952.2 | 6710 | Missense Mutation | AAG,AAT | K,N 311 | NP_001156424.1 | |
NM_001162953.2 | 6710 | Missense Mutation | AAG,AAT | K,N 910 | NP_001156425.1 | |
NM_001289608.1 | 6710 | Missense Mutation | AAG,AAT | K,N 877 | NP_001276537.1 | |
NM_001289609.1 | 6710 | Missense Mutation | AAG,AAT | K,N 230 | NP_001276538.1 | |
NM_001289610.1 | 6710 | Missense Mutation | AAG,AAT | K,N 311 | NP_001276539.1 | |
NM_032943.4 | 6710 | Missense Mutation | AAG,AAT | K,N 885 | NP_116561.1 | |
NM_206929.3 | 6710 | Missense Mutation | AAG,AAT | K,N 351 | NP_996812.1 | |
NM_206930.3 | 6710 | Missense Mutation | AAG,AAT | K,N 340 | NP_996813.1 | |
XM_005274057.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2198 | XP_005274114.1 | |
XM_005274060.1 | 6710 | Missense Mutation | AAG,AAT | K,N 926 | XP_005274117.1 | |
XM_005274061.1 | 6710 | Missense Mutation | AAG,AAT | K,N 925 | XP_005274118.1 | |
XM_005274062.2 | 6710 | Missense Mutation | AAG,AAT | K,N 899 | XP_005274119.1 | |
XM_005274063.1 | 6710 | Missense Mutation | AAG,AAT | K,N 886 | XP_005274120.1 | |
XM_005274066.1 | 6710 | Missense Mutation | AAG,AAT | K,N 869 | XP_005274123.1 | |
XM_005274067.4 | 6710 | Missense Mutation | AAG,AAT | K,N 351 | XP_005274124.1 | |
XM_011545105.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2214 | XP_011543407.1 | |
XM_011545106.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2213 | XP_011543408.1 | |
XM_011545107.2 | 6710 | Missense Mutation | AAG,AAT | K,N 2187 | XP_011543409.1 | |
XM_011545108.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2174 | XP_011543410.1 | |
XM_011545109.2 | 6710 | Missense Mutation | AAG,AAT | K,N 2165 | XP_011543411.1 | |
XM_011545110.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2157 | XP_011543412.1 | |
XM_011545112.1 | 6710 | Intron | XP_011543414.1 | |||
XM_011545114.2 | 6710 | Missense Mutation | AAG,AAT | K,N 340 | XP_011543416.1 | |
XM_011545115.1 | 6710 | Missense Mutation | AAG,AAT | K,N 300 | XP_011543417.1 | |
XM_011545116.2 | 6710 | Missense Mutation | AAG,AAT | K,N 300 | XP_011543418.1 | |
XM_017017933.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2197 | XP_016873422.1 | |
XM_017017934.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2186 | XP_016873423.1 | |
XM_017017935.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2146 | XP_016873424.1 | |
XM_017017936.1 | 6710 | Missense Mutation | AAG,AAT | K,N 2071 | XP_016873425.1 | |
XM_017017937.1 | 6710 | Missense Mutation | AAG,AAT | K,N 851 | XP_016873426.1 | |
XM_017017938.1 | 6710 | Missense Mutation | AAG,AAT | K,N 837 | XP_016873427.1 | |
XM_017017939.1 | 6710 | Missense Mutation | AAG,AAT | K,N 420 | XP_016873428.1 | |
XM_017017940.1 | 6710 | Missense Mutation | AAG,AAT | K,N 404 | XP_016873429.1 |