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ACCTGTAATCCCGGCGACTCGGAAC[G/T]CTGAGACGGGCGGATCGCTTGAACC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610963 MIM: 606477 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMG6 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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SMG6 - SMG6, nonsense mediated mRNA decay factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256827.1 | Intron | NP_001243756.1 | ||||
NM_001256828.1 | Intron | NP_001243757.1 | ||||
NM_001282326.1 | Intron | NP_001269255.1 | ||||
NM_017575.4 | Intron | NP_060045.4 | ||||
XM_005256569.3 | Intron | XP_005256626.1 | ||||
XM_005256570.3 | Intron | XP_005256627.1 | ||||
XM_005256571.4 | Intron | XP_005256628.1 | ||||
XM_011523769.2 | Intron | XP_011522071.1 | ||||
XM_011523772.2 | Intron | XP_011522074.1 | ||||
XM_011523773.2 | Intron | XP_011522075.1 | ||||
XM_011523774.2 | Intron | XP_011522076.1 | ||||
XM_011523775.2 | Intron | XP_011522077.1 | ||||
XM_017024398.1 | Intron | XP_016879887.1 | ||||
XM_017024399.1 | Intron | XP_016879888.1 |
SRR - serine racemase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304803.1 | Intron | NP_001291732.1 | ||||
NM_021947.2 | Intron | NP_068766.1 | ||||
XM_006721565.3 | Intron | XP_006721628.1 | ||||
XM_006721566.3 | Intron | XP_006721629.1 | ||||
XM_011523974.2 | Intron | XP_011522276.1 |