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CAGGACCACGAACGTCCCGACCCCC[A/G]GCAGCAAGAGGCCGCCCAGGGCCCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 158372 | |||||||||||||||||||||||
Literature Links: |
MUC4 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 - 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 |
MUC4 - mucin 4, cell surface associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322468.1 | 22322 | Missense Mutation | NP_001309397.1 | |||
NM_004532.5 | 22322 | Missense Mutation | CCG,CTG | P,L 1147 | NP_004523.3 | |
NM_018406.6 | 22322 | Intron | NP_060876.5 | |||
NM_138297.4 | 22322 | Missense Mutation | CCG,CTG | P,L 1096 | NP_612154.2 |