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TTGTAGGTACATGCCTTCAGCTGAA[C/T]GAGACCTTGAGCAGCATGAAGACAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601756 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GALNT3 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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GALNT3 - polypeptide N-acetylgalactosaminyltransferase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004482.3 | 1975 | Missense Mutation | ATT,GTT | I,V 569 | NP_004473.2 | |
XM_005246449.1 | 1975 | Missense Mutation | ATT,GTT | I,V 569 | XP_005246506.1 | |
XM_011510929.1 | 1975 | Missense Mutation | ATT,GTT | I,V 569 | XP_011509231.1 | |
XM_017003770.1 | 1975 | Missense Mutation | ATT,GTT | I,V 569 | XP_016859259.1 |