Product Details

SNP ID

rs202199122

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:45218249 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGGCCAGGGCCTGGGCACCCAGC[A/G]TGCCCACGATGCCATCCAGGGCCTC

Phenotype

MIM: 616927

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

EXOC3L2 PubMed Links

Gene Details

Gene

EXOC3L2

Gene Name

exocyst complex component 3 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_138568.3	652	Missense Mutation	ACG,ATG	T204M	NP_612635.3

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