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GCTCGAAGACCTGCTTCACATTGAT[A/G]TTCTCCTTGGCACTGGCTTCAAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604350 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAB3D 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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RAB3D - RAB3D, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004283.3 | 768 | Silent Mutation | AAC,AAT | N,N 169 | NP_004274.1 |
TSPAN16 - tetraspanin 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282509.1 | 768 | Intron | NP_001269438.1 | |||
NM_001282510.1 | 768 | Intron | NP_001269439.1 | |||
NM_012466.3 | 768 | Intron | NP_036598.1 | |||
XM_011527901.1 | 768 | Intron | XP_011526203.1 | |||
XM_011527902.1 | 768 | Intron | XP_011526204.1 | |||
XM_011527903.2 | 768 | Intron | XP_011526205.1 |