Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCAGCCTCTCAGGTGAACCAAGCC[G/T]CTATGCCGCGTGTCTGGTACCTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 136836 MIM: 602018 | ||||||||||||||||||||
Literature Links: |
FUT6 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 |
FUT6 - fucosyltransferase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000150.2 | 2398 | Missense Mutation | NP_000141.1 | |||
NM_001040701.1 | 2398 | Missense Mutation | NP_001035791.1 | |||
XM_005259526.4 | 2398 | Missense Mutation | XP_005259583.1 | |||
XM_005259527.3 | 2398 | Intron | XP_005259584.1 | |||
XM_011527868.2 | 2398 | Missense Mutation | XP_011526170.1 | |||
XM_011527869.2 | 2398 | Missense Mutation | XP_011526171.1 | |||
XM_011527870.2 | 2398 | Missense Mutation | XP_011526172.1 | |||
XM_011527872.2 | 2398 | Missense Mutation | XP_011526174.1 | |||
XM_011527873.2 | 2398 | Missense Mutation | XP_011526175.1 | |||
XM_011527874.2 | 2398 | Missense Mutation | XP_011526176.1 | |||
XM_011527875.2 | 2398 | Missense Mutation | XP_011526177.1 | |||
XM_011527876.2 | 2398 | Missense Mutation | XP_011526178.1 | |||
XM_011527878.2 | 2398 | Missense Mutation | XP_011526180.1 | |||
XM_011527879.2 | 2398 | Missense Mutation | XP_011526181.1 |
NRTN - neurturin | ||||||
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There are no transcripts associated with this gene. |