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ATATCCGGGAGTCCTGGAGGCGGCT[A/G]GAGCCATTACTGCCCACAATGGGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 604013 MIM: 601019 | ||||||||||||||||||||
Literature Links: |
B4GALT2 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 |
B4GALT2 - beta-1,4-galactosyltransferase 2 | ||||||
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There are no transcripts associated with this gene. |
CCDC24 - coiled-coil domain containing 24 | ||||||
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There are no transcripts associated with this gene. |
SLC6A9 - solute carrier family 6 member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024845.2 | 2301 | Silent Mutation | TCC,TCT | S,S 625 | NP_001020016.1 | |
NM_001261380.1 | 2301 | Silent Mutation | TCC,TCT | S,S 629 | NP_001248309.1 | |
NM_006934.3 | 2301 | Silent Mutation | TCC,TCT | S,S 644 | NP_008865.2 | |
NM_201649.3 | 2301 | Silent Mutation | TCC,TCT | S,S 698 | NP_964012.2 | |
XM_011542017.2 | 2301 | Intron | XP_011540319.1 | |||
XM_017002151.1 | 2301 | Silent Mutation | TCC,TCT | S,S 625 | XP_016857640.1 | |
XM_017002152.1 | 2301 | Silent Mutation | TCC,TCT | S,S 598 | XP_016857641.1 | |
XM_017002153.1 | 2301 | Silent Mutation | TCC,TCT | S,S 587 | XP_016857642.1 |