Product Details

SNP ID

rs112099561

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:39897575 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCTCAGCGCCAAGAATCGCGAAC[A/G]CAGGTCATTCCGCCTCTTGCGCTCC

Phenotype

MIM: 164850

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MYCL PubMed Links

Gene Details

Gene

MYCL

Gene Name

v-myc avian myelocytomatosis viral oncogene lung carcinoma derived homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033081.2	1473	Missense Mutation	CGT,TGT	R298C	NP_001028253.1
NM_001033082.2	1473	Missense Mutation	CGT,TGT	R328C	NP_001028254.2
NM_005376.4	1473	Intron			NP_005367.2

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