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AGGACAGCTGGAAAGACATGGAGCC[C/T]CAGCTGGCAGAGATGATTAAGCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608442 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SYNE2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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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
|
SYNE2 - spectrin repeat containing nuclear envelope protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015180.4 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | NP_055995.4 | |
NM_182910.2 | 17775 | Intron | NP_878914.1 | |||
NM_182913.2 | 17775 | Intron | NP_878917.1 | |||
NM_182914.2 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | NP_878918.2 | |
XM_005267454.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_005267511.1 | |
XM_005267456.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_005267513.1 | |
XM_005267457.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_005267514.1 | |
XM_005267458.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_005267515.1 | |
XM_005267459.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_005267516.1 | |
XM_011536574.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534876.1 | |
XM_011536575.2 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534877.1 | |
XM_011536576.2 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534878.1 | |
XM_011536577.2 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534879.1 | |
XM_011536578.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534880.1 | |
XM_011536579.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534881.1 | |
XM_011536580.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534882.1 | |
XM_011536581.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_011534883.1 | |
XM_011536582.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5757 | XP_011534884.1 | |
XM_011536584.2 | 17775 | Intron | XP_011534886.1 | |||
XM_017021101.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5796 | XP_016876590.1 | |
XM_017021102.1 | 17775 | Silent Mutation | CCC,CCT | P,P 5773 | XP_016876591.1 | |
XM_017021103.1 | 17775 | Intron | XP_016876592.1 | |||
XM_017021104.1 | 17775 | Intron | XP_016876593.1 |