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GTCCAGGGCGCAGATCTGGGCTCTG[G/T]TGTCTGGTGTCGGAGGGTTTGGAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CLDN10 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 |
CLDN10 - claudin 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001160100.1 | 263 | Missense Mutation | GTG,TTG | V,L 10 | NP_001153572.1 | |
NM_006984.4 | 263 | Intron | NP_008915.1 | |||
NM_182848.3 | 263 | Missense Mutation | GTG,TTG | V,L 10 | NP_878268.1 | |
XM_011521134.2 | 263 | Intron | XP_011519436.1 | |||
XM_017020843.1 | 263 | Missense Mutation | GTG,TTG | V,L 10 | XP_016876332.1 | |
XM_017020844.1 | 263 | Missense Mutation | GTG,TTG | V,L 10 | XP_016876333.1 |