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GGCGGAGGTGGGGTCAGTGCCGTGC[A/G]TGTTTGATCCAGTTTCTGATCATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606251 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GALNT9 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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GALNT9 - polypeptide N-acetylgalactosaminyltransferase 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122636.1 | 980 | Silent Mutation | NP_001116108.1 | |||
NM_021808.3 | 980 | Silent Mutation | NP_068580.2 | |||
XM_017019371.1 | 980 | Silent Mutation | XP_016874860.1 | |||
XM_017019372.1 | 980 | Silent Mutation | XP_016874861.1 | |||
XM_017019373.1 | 980 | Silent Mutation | XP_016874862.1 | |||
XM_017019374.1 | 980 | Silent Mutation | XP_016874863.1 | |||
XM_017019375.1 | 980 | Intron | XP_016874864.1 | |||
XM_017019376.1 | 980 | Intron | XP_016874865.1 |