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ATCCAGTGCCACCAACGGAAACCAT[A/G]TCTGAGGTTTCGGGGGCCACAGTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SAMD15 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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SAMD15 - sterile alpha motif domain containing 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010860.1 | 504 | Missense Mutation | ATA,ATG | I,M 168 | NP_001010860.1 |
TMED8 - transmembrane p24 trafficking protein family member 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_213601.1 | 504 | Intron | NP_998766.1 | |||
XM_017021223.1 | 504 | Intron | XP_016876712.1 | |||
XM_017021224.1 | 504 | Intron | XP_016876713.1 | |||
XM_017021225.1 | 504 | Intron | XP_016876714.1 |