Product Details

SNP ID

rs77140803

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:77051098 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTGTTGTTCCAAAACAGAAAAAA[A/C]CAGCCACTGAACAGCAGTAGCGACA

Phenotype

MIM: 610392

Polymorphism

A/C, Transversion 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	13955	Missense Mutation	GGT,GTT	G4607V	NP_055872.4
XM_005266299.2	13955	Missense Mutation	GGT,GTT	G4684V	XP_005266356.1
XM_006719779.2	13955	Missense Mutation	GGT,GTT	G4726V	XP_006719842.1
XM_006719780.2	13955	Missense Mutation	GGT,GTT	G4723V	XP_006719843.1
XM_006719781.2	13955	Missense Mutation	GGT,GTT	G4718V	XP_006719844.1
XM_006719782.2	13955	Missense Mutation	GGT,GTT	G4701V	XP_006719845.1
XM_006719783.2	13955	Missense Mutation	GGT,GTT	G4692V	XP_006719846.1
XM_006719784.2	13955	Missense Mutation	GGT,GTT	G4690V	XP_006719847.1
XM_006719785.2	13955	Missense Mutation	GGT,GTT	G4666V	XP_006719848.1
XM_006719786.2	13955	Missense Mutation	GGT,GTT	G4632V	XP_006719849.1
XM_006719787.2	13955	Missense Mutation	GGT,GTT	G4626V	XP_006719850.1
XM_006719788.2	13955	Missense Mutation	GGT,GTT	G4618V	XP_006719851.1
XM_006719789.2	13955	Missense Mutation	GGT,GTT	G4681V	XP_006719852.1
XM_011535004.2	13955	Missense Mutation	GGT,GTT	G4617V	XP_011533306.1
XM_011535005.2	13955	Missense Mutation	GGT,GTT	G3771V	XP_011533307.1
XM_017020454.1	13955	Missense Mutation	GGT,GTT	G4707V	XP_016875943.1
XM_017020455.1	13955	Missense Mutation	GGT,GTT	G4682V	XP_016875944.1
XM_017020456.1	13955	Missense Mutation	GGT,GTT	G4665V	XP_016875945.1
XM_017020457.1	13955	Missense Mutation	GGT,GTT	G4659V	XP_016875946.1
XM_017020458.1	13955	Missense Mutation	GGT,GTT	G4648V	XP_016875947.1
XM_017020459.1	13955	Missense Mutation	GGT,GTT	G4596V	XP_016875948.1
XM_017020460.1	13955	Missense Mutation	GGT,GTT	G4592V	XP_016875949.1
XM_017020461.1	13955	Missense Mutation	GGT,GTT	G4588V	XP_016875950.1
XM_017020462.1	13955	Missense Mutation	GGT,GTT	G4584V	XP_016875951.1
XM_017020463.1	13955	Missense Mutation	GGT,GTT	G4571V	XP_016875952.1
XM_017020464.1	13955	Missense Mutation	GGT,GTT	G4566V	XP_016875953.1
XM_017020465.1	13955	Missense Mutation	GGT,GTT	G4548V	XP_016875954.1
XM_017020466.1	13955	Missense Mutation	GGT,GTT	G4532V	XP_016875955.1
XM_017020467.1	13955	Missense Mutation	GGT,GTT	G4529V	XP_016875956.1
XM_017020468.1	13955	Missense Mutation	GGT,GTT	G4461V	XP_016875957.1

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