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AGTATAGCCCCAGGGTCCTGCACTT[C/T]GCCTTGGAGGAGCCCAGGTGTGATT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 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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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152499.2 | 385 | Silent Mutation | TTC,TTT | F,F 117 | NP_689712.1 | |
XM_017000423.1 | 385 | Silent Mutation | TTC,TTT | F,F 198 | XP_016855912.1 | |
XM_017000424.1 | 385 | Silent Mutation | TTC,TTT | F,F 198 | XP_016855913.1 | |
XM_017000425.1 | 385 | Silent Mutation | TTC,TTT | F,F 198 | XP_016855914.1 | |
XM_017000426.1 | 385 | Silent Mutation | TTC,TTT | F,F 167 | XP_016855915.1 | |
XM_017000427.1 | 385 | Silent Mutation | TTC,TTT | F,F 166 | XP_016855916.1 | |
XM_017000428.1 | 385 | Silent Mutation | TTC,TTT | F,F 166 | XP_016855917.1 | |
XM_017000429.1 | 385 | Silent Mutation | TTC,TTT | F,F 162 | XP_016855918.1 | |
XM_017000430.1 | 385 | Silent Mutation | TTC,TTT | F,F 166 | XP_016855919.1 | |
XM_017000431.1 | 385 | Silent Mutation | TTC,TTT | F,F 130 | XP_016855920.1 | |
XM_017000432.1 | 385 | Silent Mutation | TTC,TTT | F,F 118 | XP_016855921.1 | |
XM_017000433.1 | 385 | Silent Mutation | TTC,TTT | F,F 117 | XP_016855922.1 | |
XM_017000434.1 | 385 | Silent Mutation | TTC,TTT | F,F 117 | XP_016855923.1 | |
XM_017000435.1 | 385 | Intron | XP_016855924.1 | |||
XM_017000436.1 | 385 | Intron | XP_016855925.1 | |||
XM_017000437.1 | 385 | Silent Mutation | TTC,TTT | F,F 99 | XP_016855926.1 | |
XM_017000438.1 | 385 | Silent Mutation | TTC,TTT | F,F 94 | XP_016855927.1 | |
XM_017000439.1 | 385 | Silent Mutation | TTC,TTT | F,F 86 | XP_016855928.1 | |
XM_017000440.1 | 385 | Silent Mutation | TTC,TTT | F,F 81 | XP_016855929.1 | |
XM_017000441.1 | 385 | Silent Mutation | TTC,TTT | F,F 81 | XP_016855930.1 | |
XM_017000442.1 | 385 | Intron | XP_016855931.1 | |||
XM_017000443.1 | 385 | Silent Mutation | TTC,TTT | F,F 166 | XP_016855932.1 | |
XM_017000444.1 | 385 | Silent Mutation | TTC,TTT | F,F 166 | XP_016855933.1 | |
XM_017000445.1 | 385 | UTR 5 | XP_016855934.1 | |||
XM_017000446.1 | 385 | UTR 5 | XP_016855935.1 |
SLC6A9 - solute carrier family 6 member 9 | ||||||
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There are no transcripts associated with this gene. |