Product Details

SNP ID

rs73760024

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:19477402 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAACAATTATCATGTGGACAAACA[A/G]AAAAAAAATCTCTGTGAAAATGGTA

Phenotype

MIM: 603019

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CDH18 PubMed Links

Additional Information

For this assay, SNP(s) [rs375503594] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CDH18

Gene Name

cadherin 18

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

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