Product Details

SNP ID

rs201311103

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:77051091 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACAAAAATGTGTTGTTCCAAAACA[A/G]AAAAAAACAGCCACTGAACAGCAGT

Phenotype

MIM: 610392

Polymorphism

A/G, 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	13962	Silent Mutation	TTC,TTT	F4609F	NP_055872.4
XM_005266299.2	13962	Silent Mutation	TTC,TTT	F4686F	XP_005266356.1
XM_006719779.2	13962	Silent Mutation	TTC,TTT	F4728F	XP_006719842.1
XM_006719780.2	13962	Silent Mutation	TTC,TTT	F4725F	XP_006719843.1
XM_006719781.2	13962	Silent Mutation	TTC,TTT	F4720F	XP_006719844.1
XM_006719782.2	13962	Silent Mutation	TTC,TTT	F4703F	XP_006719845.1
XM_006719783.2	13962	Silent Mutation	TTC,TTT	F4694F	XP_006719846.1
XM_006719784.2	13962	Silent Mutation	TTC,TTT	F4692F	XP_006719847.1
XM_006719785.2	13962	Silent Mutation	TTC,TTT	F4668F	XP_006719848.1
XM_006719786.2	13962	Silent Mutation	TTC,TTT	F4634F	XP_006719849.1
XM_006719787.2	13962	Silent Mutation	TTC,TTT	F4628F	XP_006719850.1
XM_006719788.2	13962	Silent Mutation	TTC,TTT	F4620F	XP_006719851.1
XM_006719789.2	13962	Silent Mutation	TTC,TTT	F4683F	XP_006719852.1
XM_011535004.2	13962	Silent Mutation	TTC,TTT	F4619F	XP_011533306.1
XM_011535005.2	13962	Silent Mutation	TTC,TTT	F3773F	XP_011533307.1
XM_017020454.1	13962	Silent Mutation	TTC,TTT	F4709F	XP_016875943.1
XM_017020455.1	13962	Silent Mutation	TTC,TTT	F4684F	XP_016875944.1
XM_017020456.1	13962	Silent Mutation	TTC,TTT	F4667F	XP_016875945.1
XM_017020457.1	13962	Silent Mutation	TTC,TTT	F4661F	XP_016875946.1
XM_017020458.1	13962	Silent Mutation	TTC,TTT	F4650F	XP_016875947.1
XM_017020459.1	13962	Silent Mutation	TTC,TTT	F4598F	XP_016875948.1
XM_017020460.1	13962	Silent Mutation	TTC,TTT	F4594F	XP_016875949.1
XM_017020461.1	13962	Silent Mutation	TTC,TTT	F4590F	XP_016875950.1
XM_017020462.1	13962	Silent Mutation	TTC,TTT	F4586F	XP_016875951.1
XM_017020463.1	13962	Silent Mutation	TTC,TTT	F4573F	XP_016875952.1
XM_017020464.1	13962	Silent Mutation	TTC,TTT	F4568F	XP_016875953.1
XM_017020465.1	13962	Silent Mutation	TTC,TTT	F4550F	XP_016875954.1
XM_017020466.1	13962	Silent Mutation	TTC,TTT	F4534F	XP_016875955.1
XM_017020467.1	13962	Silent Mutation	TTC,TTT	F4531F	XP_016875956.1
XM_017020468.1	13962	Silent Mutation	TTC,TTT	F4463F	XP_016875957.1

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