Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTCTGGAAGACCTGGTTGGCAGCC[A/T]TGCTGAAGAGGAAGTCCACCTCGTC
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 |
---|---|---|
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 |
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 | 1093 | Missense Mutation | AAG,ATG | K,M 172 | NP_892019.2 | |
XM_011518633.1 | 1093 | Missense Mutation | AAG,ATG | K,M 208 | XP_011516935.1 | |
XM_011518634.1 | 1093 | Missense Mutation | AAG,ATG | K,M 208 | XP_011516936.1 | |
XM_011518635.1 | 1093 | Missense Mutation | AAG,ATG | K,M 208 | XP_011516937.1 | |
XM_011518636.1 | 1093 | Missense Mutation | AAG,ATG | K,M 208 | XP_011516938.1 | |
XM_011518637.1 | 1093 | Missense Mutation | AAG,ATG | K,M 172 | XP_011516939.1 | |
XM_011518638.2 | 1093 | Missense Mutation | AAG,ATG | K,M 140 | XP_011516940.1 |
LOC102723971 - lipocalin 1-like | ||||||
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There are no transcripts associated with this gene. |