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CTTCACTTCAGGTCTGATATCCCTC[C/T]GGTACTTGAGCTCCTCAGCAGCAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603019 | ||||||||||||||||||||
Literature Links: |
CDH18 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 |
CDH18 - cadherin 18 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167667.1 | 3054 | UTR 3 | NP_001161139.1 | |||
NM_001291956.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | NP_001278885.1 | |
NM_001291957.1 | 3054 | UTR 3 | NP_001278886.1 | |||
NM_004934.3 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | NP_004925.1 | |
XM_005248228.3 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_005248285.1 | |
XM_006714435.3 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_006714498.1 | |
XM_011513928.2 | 3054 | Missense Mutation | CAG,CGG | Q,R 622 | XP_011512230.1 | |
XM_011513929.2 | 3054 | Missense Mutation | CAG,CGG | Q,R 520 | XP_011512231.1 | |
XM_011513930.2 | 3054 | UTR 3 | XP_011512232.1 | |||
XM_017008924.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864413.1 | |
XM_017008925.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864414.1 | |
XM_017008926.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864415.1 | |
XM_017008927.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864416.1 | |
XM_017008928.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864417.1 | |
XM_017008929.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864418.1 | |
XM_017008930.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864419.1 | |
XM_017008931.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864420.1 | |
XM_017008932.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 688 | XP_016864421.1 | |
XM_017008933.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 465 | XP_016864422.1 | |
XM_017008934.1 | 3054 | Missense Mutation | CAG,CGG | Q,R 465 | XP_016864423.1 | |
XM_017008935.1 | 3054 | UTR 3 | XP_016864424.1 | |||
XM_017008936.1 | 3054 | UTR 3 | XP_016864425.1 | |||
XM_017008937.1 | 3054 | UTR 3 | XP_016864426.1 | |||
XM_017008938.1 | 3054 | UTR 3 | XP_016864427.1 | |||
XM_017008939.1 | 3054 | UTR 3 | XP_016864428.1 | |||
XM_017008940.1 | 3054 | UTR 3 | XP_016864429.1 | |||
XM_017008941.1 | 3054 | UTR 3 | XP_016864430.1 |