Product Details

SNP ID
rs17852884
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:19473593 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCAAGGCTGTGATGTCAAAGGCC[C/T]CTGTGTCTTCCTCTCCGCCTCCTTC
Phenotype
MIM: 603019
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CDH18 PubMed Links

Gene Details

Gene
CDH18
Gene Name
cadherin 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001167667.1 2997 UTR 3 NP_001161139.1
NM_001291956.1 2997 Missense Mutation GAG,GGG E669G NP_001278885.1
NM_001291957.1 2997 UTR 3 NP_001278886.1
NM_004934.3 2997 Missense Mutation GAG,GGG E669G NP_004925.1
XM_005248228.3 2997 Missense Mutation GAG,GGG E669G XP_005248285.1
XM_006714435.3 2997 Missense Mutation GAG,GGG E669G XP_006714498.1
XM_011513928.2 2997 Missense Mutation GAG,GGG E603G XP_011512230.1
XM_011513929.2 2997 Missense Mutation GAG,GGG E501G XP_011512231.1
XM_011513930.2 2997 UTR 3 XP_011512232.1
XM_017008924.1 2997 Missense Mutation GAG,GGG E669G XP_016864413.1
XM_017008925.1 2997 Missense Mutation GAG,GGG E669G XP_016864414.1
XM_017008926.1 2997 Missense Mutation GAG,GGG E669G XP_016864415.1
XM_017008927.1 2997 Missense Mutation GAG,GGG E669G XP_016864416.1
XM_017008928.1 2997 Missense Mutation GAG,GGG E669G XP_016864417.1
XM_017008929.1 2997 Missense Mutation GAG,GGG E669G XP_016864418.1
XM_017008930.1 2997 Missense Mutation GAG,GGG E669G XP_016864419.1
XM_017008931.1 2997 Missense Mutation GAG,GGG E669G XP_016864420.1
XM_017008932.1 2997 Missense Mutation GAG,GGG E669G XP_016864421.1
XM_017008933.1 2997 Missense Mutation GAG,GGG E446G XP_016864422.1
XM_017008934.1 2997 Missense Mutation GAG,GGG E446G XP_016864423.1
XM_017008935.1 2997 UTR 3 XP_016864424.1
XM_017008936.1 2997 UTR 3 XP_016864425.1
XM_017008937.1 2997 UTR 3 XP_016864426.1
XM_017008938.1 2997 UTR 3 XP_016864427.1
XM_017008939.1 2997 UTR 3 XP_016864428.1
XM_017008940.1 2997 UTR 3 XP_016864429.1
XM_017008941.1 2997 UTR 3 XP_016864430.1

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