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CAGGAACGTAAAGACCGAAGGGTGG[G/T]TTTCGAAGGAGCGGATTTCGAAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602655 MIM: 612762 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC4A1AP 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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SLC4A1AP - solute carrier family 4 member 1 adaptor protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018158.2 | 406 | Missense Mutation | GTT,TTT | V,F 42 | NP_060628.2 |
SUPT7L - SPT7-like STAGA complex gamma subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282729.1 | 406 | Intron | NP_001269658.1 | |||
NM_001282730.1 | 406 | Intron | NP_001269659.1 | |||
NM_001282731.1 | 406 | Intron | NP_001269660.1 | |||
NM_001282732.1 | 406 | Intron | NP_001269661.1 | |||
NM_014860.2 | 406 | Intron | NP_055675.1 | |||
XM_005264672.4 | 406 | Intron | XP_005264729.1 |