Product Details

SNP ID

rs201330064

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:128801205 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGCAGGTGAGCTGCGTTCTCTACG[A/G]GAGGAGATTTCCCTGTTAGAGCATG

Phenotype

MIM: 611902

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CCDC136 PubMed Links

Gene Details

Gene

CCDC136

Gene Name

coiled-coil domain containing 136

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001201372.1	566	Silent Mutation	CGA,CGG	R172R	NP_001188301.1
NM_022742.4	566	Silent Mutation	CGA,CGG	R122R	NP_073579.4
XM_005250534.3	566	Silent Mutation	CGA,CGG	R172R	XP_005250591.1
XM_005250538.1	566	Silent Mutation	CGA,CGG	R172R	XP_005250595.1
XM_011516483.1	566	Silent Mutation	CGA,CGG	R172R	XP_011514785.1
XM_011516484.1	566	Silent Mutation	CGA,CGG	R172R	XP_011514786.1
XM_011516485.1	566	Silent Mutation	CGA,CGG	R172R	XP_011514787.1
XM_011516486.1	566	Silent Mutation	CGA,CGG	R172R	XP_011514788.1
XM_011516487.2	566	Silent Mutation	CGA,CGG	R172R	XP_011514789.1
XM_011516488.2	566	Silent Mutation	CGA,CGG	R172R	XP_011514790.1
XM_011516489.1	566	Silent Mutation	CGA,CGG	R172R	XP_011514791.1
XM_011516490.2	566	Silent Mutation	CGA,CGG	R172R	XP_011514792.1
XM_017012532.1	566	Silent Mutation	CGA,CGG	R172R	XP_016868021.1
XM_017012533.1	566	Silent Mutation	CGA,CGG	R122R	XP_016868022.1
XM_017012534.1	566	Silent Mutation	CGA,CGG	R172R	XP_016868023.1
XM_017012535.1	566	Silent Mutation	CGA,CGG	R172R	XP_016868024.1
XM_017012536.1	566	Silent Mutation	CGA,CGG	R172R	XP_016868025.1

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