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Search Thermo Fisher Scientific
CAGACACTTGGAGTCAGGCAAGAAG[A/G]CTGTGGAGCCCAGAGGCCCCAGCTG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 733 | Missense Mutation | GCC,GTC | A,V 518 | NP_001116108.1 | |
NM_021808.3 | 733 | Missense Mutation | GCC,GTC | A,V 152 | NP_068580.2 | |
XM_017019371.1 | 733 | Missense Mutation | GCC,GTC | A,V 417 | XP_016874860.1 | |
XM_017019372.1 | 733 | Missense Mutation | GCC,GTC | A,V 415 | XP_016874861.1 | |
XM_017019373.1 | 733 | Missense Mutation | GCC,GTC | A,V 415 | XP_016874862.1 | |
XM_017019374.1 | 733 | Missense Mutation | GCC,GTC | A,V 375 | XP_016874863.1 | |
XM_017019375.1 | 733 | Intron | XP_016874864.1 | |||
XM_017019376.1 | 733 | Intron | XP_016874865.1 |