Product Details

SNP ID
rs140353037
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:19473536 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTCACTTCAGGTCTGATATCCCTC[C/T]GGTACTTGAGCTCCTCAGCAGCAGA
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 3054 UTR 3 NP_001161139.1
NM_001291956.1 3054 Missense Mutation CAG,CGG Q688R NP_001278885.1
NM_001291957.1 3054 UTR 3 NP_001278886.1
NM_004934.3 3054 Missense Mutation CAG,CGG Q688R NP_004925.1
XM_005248228.3 3054 Missense Mutation CAG,CGG Q688R XP_005248285.1
XM_006714435.3 3054 Missense Mutation CAG,CGG Q688R XP_006714498.1
XM_011513928.2 3054 Missense Mutation CAG,CGG Q622R XP_011512230.1
XM_011513929.2 3054 Missense Mutation CAG,CGG Q520R XP_011512231.1
XM_011513930.2 3054 UTR 3 XP_011512232.1
XM_017008924.1 3054 Missense Mutation CAG,CGG Q688R XP_016864413.1
XM_017008925.1 3054 Missense Mutation CAG,CGG Q688R XP_016864414.1
XM_017008926.1 3054 Missense Mutation CAG,CGG Q688R XP_016864415.1
XM_017008927.1 3054 Missense Mutation CAG,CGG Q688R XP_016864416.1
XM_017008928.1 3054 Missense Mutation CAG,CGG Q688R XP_016864417.1
XM_017008929.1 3054 Missense Mutation CAG,CGG Q688R XP_016864418.1
XM_017008930.1 3054 Missense Mutation CAG,CGG Q688R XP_016864419.1
XM_017008931.1 3054 Missense Mutation CAG,CGG Q688R XP_016864420.1
XM_017008932.1 3054 Missense Mutation CAG,CGG Q688R XP_016864421.1
XM_017008933.1 3054 Missense Mutation CAG,CGG Q465R XP_016864422.1
XM_017008934.1 3054 Missense Mutation CAG,CGG Q465R 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

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