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CCTGCGGGCAGGGCATCCTGTAGCC[A/T]CGCTCCACCTGCTCCAGCACCTCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137025 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FYN PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FYN - FYN proto-oncogene, Src family tyrosine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002037.5 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | NP_002028.1 | |
NM_153047.3 | 1546 | Silent Mutation | CGA,CGT | R,R 478 | NP_694592.1 | |
NM_153048.3 | 1546 | Silent Mutation | CGA,CGT | R,R 426 | NP_694593.1 | |
XM_005266890.3 | 1546 | Silent Mutation | CGA,CGT | R,R 478 | XP_005266947.1 | |
XM_005266892.3 | 1546 | Silent Mutation | CGA,CGT | R,R 426 | XP_005266949.1 | |
XM_017010650.1 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | XP_016866139.1 | |
XM_017010651.1 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | XP_016866140.1 | |
XM_017010652.1 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | XP_016866141.1 | |
XM_017010653.1 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | XP_016866142.1 | |
XM_017010654.1 | 1546 | Silent Mutation | CGA,CGT | R,R 481 | XP_016866143.1 | |
XM_017010655.1 | 1546 | Intron | XP_016866144.1 |