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AGCAGCCACCTCACAGATCAGGACA[A/G]TGAAATCCGAGCCACTGACCTGCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601333 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SUPT6H 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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SUPT6H - SPT6 homolog, histone chaperone | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320755.1 | 1138 | Missense Mutation | AAT,AGT | N,S 287 | NP_001307684.1 | |
NM_003170.4 | 1138 | Missense Mutation | AAT,AGT | N,S 287 | NP_003161.2 | |
XM_017024978.1 | 1138 | Missense Mutation | AAT,AGT | N,S 287 | XP_016880467.1 | |
XM_017024979.1 | 1138 | Missense Mutation | AAT,AGT | N,S 287 | XP_016880468.1 | |
XM_017024980.1 | 1138 | Missense Mutation | AAT,AGT | N,S 164 | XP_016880469.1 |