Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCTCCGGTCTCCATAGAGGCTG[G/T]GTCAGCAGTGGGCAAAACAACTTCC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||
Phenotype: |
MIM: 610360 | |||||||||||||||||||||||
Literature Links: |
MUC20 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
MUC20 - mucin 20, cell surface associated | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282506.1 | 1796 | Missense Mutation | GGG,GTG | G,V 557 | NP_001269435.1 | |
NM_001291833.1 | 1796 | Missense Mutation | GGG,GTG | G,V 383 | NP_001278762.1 | |
NM_020790.1 | 1796 | Missense Mutation | GGG,GTG | G,V 403 | NP_065841.1 | |
NM_152673.3 | 1796 | Missense Mutation | GGG,GTG | G,V 386 | NP_689886.3 |