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AATATTATGGGGTGTGCCACCAACC[A/G]TCAAGTTGCCATAATAGAAATCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613699 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLT6D1 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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GLT6D1 - glycosyltransferase 6 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182974.2 | 1270 | Missense Mutation | ACG,ATG | T,M 231 | NP_892019.2 | |
XM_011518633.1 | 1270 | Missense Mutation | ACG,ATG | T,M 267 | XP_011516935.1 | |
XM_011518634.1 | 1270 | Missense Mutation | ACG,ATG | T,M 267 | XP_011516936.1 | |
XM_011518635.1 | 1270 | Missense Mutation | ACG,ATG | T,M 267 | XP_011516937.1 | |
XM_011518636.1 | 1270 | Missense Mutation | ACG,ATG | T,M 267 | XP_011516938.1 | |
XM_011518637.1 | 1270 | Missense Mutation | ACG,ATG | T,M 231 | XP_011516939.1 | |
XM_011518638.2 | 1270 | Missense Mutation | ACG,ATG | T,M 199 | XP_011516940.1 |
LOC102723971 - lipocalin 1-like | ||||||
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There are no transcripts associated with this gene. |