Product Details

SNP ID

rs144762909

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:77051817 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAAAATGTTCTGCCTACCTGAGC[C/T]CTGGAAACATCAGAACAGGCACCAC

Phenotype

MIM: 610392

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYCBP2 PubMed Links

Gene Details

Gene

MYCBP2

Gene Name

MYC binding protein 2, E3 ubiquitin protein ligase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015057.4	13884	Silent Mutation			NP_055872.4
XM_005266299.2	13884	Missense Mutation			XP_005266356.1
XM_006719779.2	13884	Missense Mutation			XP_006719842.1
XM_006719780.2	13884	Missense Mutation			XP_006719843.1
XM_006719781.2	13884	Missense Mutation			XP_006719844.1
XM_006719782.2	13884	Missense Mutation			XP_006719845.1
XM_006719783.2	13884	Missense Mutation			XP_006719846.1
XM_006719784.2	13884	Missense Mutation			XP_006719847.1
XM_006719785.2	13884	Missense Mutation			XP_006719848.1
XM_006719786.2	13884	Silent Mutation			XP_006719849.1
XM_006719787.2	13884	Missense Mutation			XP_006719850.1
XM_006719788.2	13884	Missense Mutation			XP_006719851.1
XM_006719789.2	13884	Missense Mutation			XP_006719852.1
XM_011535004.2	13884	Missense Mutation			XP_011533306.1
XM_011535005.2	13884	Missense Mutation			XP_011533307.1
XM_017020454.1	13884	Missense Mutation			XP_016875943.1
XM_017020455.1	13884	Missense Mutation			XP_016875944.1
XM_017020456.1	13884	Missense Mutation			XP_016875945.1
XM_017020457.1	13884	Missense Mutation			XP_016875946.1
XM_017020458.1	13884	Missense Mutation			XP_016875947.1
XM_017020459.1	13884	Missense Mutation			XP_016875948.1
XM_017020460.1	13884	Missense Mutation			XP_016875949.1
XM_017020461.1	13884	Missense Mutation			XP_016875950.1
XM_017020462.1	13884	Missense Mutation			XP_016875951.1
XM_017020463.1	13884	Missense Mutation			XP_016875952.1
XM_017020464.1	13884	Missense Mutation			XP_016875953.1
XM_017020465.1	13884	Missense Mutation			XP_016875954.1
XM_017020466.1	13884	Missense Mutation			XP_016875955.1
XM_017020467.1	13884	Missense Mutation			XP_016875956.1
XM_017020468.1	13884	Missense Mutation			XP_016875957.1

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