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TGGTGGCTTTTAAACCTGTGACTGC[A/C]GCAGACTTGAATCTGCACTTCCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300105 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMS 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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SMS - spermine synthase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258423.1 | Intron | NP_001245352.1 | ||||
NM_004595.4 | Intron | NP_004586.2 | ||||
XM_005274582.2 | Intron | XP_005274639.1 | ||||
XM_011545568.2 | Intron | XP_011543870.1 | ||||
XM_017029753.1 | Intron | XP_016885242.1 | ||||
XM_017029754.1 | Intron | XP_016885243.1 | ||||
XM_017029755.1 | Intron | XP_016885244.1 |