Search Thermo Fisher Scientific
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GGAGCAGGCTGCACAGTGGAGCAGA[A/C]ACCCTCCTAGCAGAAGAGAAAGTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CLDN22 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
CLDN22 - claudin 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001111319.1 | 1098 | Missense Mutation | TGT,TTT | C,F 181 | NP_001104789.1 |
CLDN24 - claudin 24 | ||||||
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There are no transcripts associated with this gene. |
WWC2 - WW and C2 domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024949.5 | 1098 | UTR 3 | NP_079225.5 | |||
XM_011532269.2 | 1098 | Intron | XP_011530571.1 |