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TAGTGATTTCCAGTGTGTATGTGCC[A/G]GGCATGAGCTTCTTCTTGGCCGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612570 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBN2 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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FBN2 - fibrillin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001999.3 | 9197 | Silent Mutation | CCC,CCT | P,P 2865 | NP_001990.2 | |
XM_017009228.1 | 9197 | Silent Mutation | CCC,CCT | P,P 2814 | XP_016864717.1 |