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CGAAGAAGGCGTACGAGGACATTTT[A/G]CCCCGCGGCTTGTTGGGGTCTCCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605005 MIM: 163906 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GALNT7 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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GALNT7 - polypeptide N-acetylgalactosaminyltransferase 7 | ||||||
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There are no transcripts associated with this gene. |
HMGB2 - high mobility group box 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130688.1 | 166 | Silent Mutation | GGC,GGT | G,G 11 | NP_001124160.1 | |
NM_001130689.1 | 166 | Silent Mutation | GGC,GGT | G,G 11 | NP_001124161.1 | |
NM_002129.3 | 166 | Silent Mutation | GGC,GGT | G,G 11 | NP_002120.1 |
LOC105377538 - uncharacterized LOC105377538 | ||||||
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There are no transcripts associated with this gene. |