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TGTGTCTGCTGACCTTGGTCCTCTC[A/G]CTCTTGCCCCCACAAGCTGCTGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604609 MIM: 608424 | ||||||||||||||||||||
Literature Links: |
LOC102724094 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 |
LOC102724094 - uncharacterized LOC102724094 | ||||||
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There are no transcripts associated with this gene. |
MUC12 - mucin 12, cell surface associated | ||||||
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There are no transcripts associated with this gene. |
MUC17 - mucin 17, cell surface associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040105.1 | 104 | Silent Mutation | TCA,TCG | S,S 17 | NP_001035194.1 |