Product Details

SNP ID

rs8082577

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:82112705 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTCAGGCCCTGCTTCCCTCCCTG[C/T]GCCGGCAGCCCAGAAACGGCCTTCA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CCDC57 PubMed Links

Gene Details

Gene

CCDC57

Gene Name

coiled-coil domain containing 57

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001316321.1	2998	Intron			NP_001303250.1
NM_198082.2	2998	Intron			NP_932348.2
XM_011523545.2	2998	UTR 3			XP_011521847.2
XM_011523546.2	2998	UTR 3			XP_011521848.1
XM_011523548.2	2998	UTR 3			XP_011521850.1
XM_011523549.2	2998	UTR 3			XP_011521851.1
XM_011523551.2	2998	UTR 3			XP_011521853.1
XM_011523552.2	2998	UTR 3			XP_011521854.1
XM_011523555.2	2998	UTR 3			XP_011521857.1
XM_011523556.2	2998	Intron			XP_011521858.2
XM_011523557.2	2998	UTR 3			XP_011521859.1
XM_017024462.1	2998	UTR 3			XP_016879951.1
XM_017024463.1	2998	Intron			XP_016879952.1
XM_017024464.1	2998	Intron			XP_016879953.1
XM_017024465.1	2998	UTR 3			XP_016879954.1
XM_017024466.1	2998	Intron			XP_016879955.1
XM_017024467.1	2998	UTR 3			XP_016879956.1
XM_017024468.1	2998	Intron			XP_016879957.1
XM_017024469.1	2998	UTR 3			XP_016879958.1
XM_017024470.1	2998	UTR 3			XP_016879959.1
XM_017024471.1	2998	UTR 3			XP_016879960.1
XM_017024472.1	2998	UTR 3			XP_016879961.1
XM_017024473.1	2998	Intron			XP_016879962.1
XM_017024474.1	2998	Intron			XP_016879963.1
XM_017024475.1	2998	UTR 3			XP_016879964.1
XM_017024476.1	2998	UTR 3			XP_016879965.1
XM_017024477.1	2998	UTR 3			XP_016879966.1
XM_017024478.1	2998	UTR 3			XP_016879967.1
XM_017024479.1	2998	Intron			XP_016879968.1
XM_017024480.1	2998	Intron			XP_016879969.1
XM_017024481.1	2998	Intron			XP_016879970.1
XM_017024482.1	2998	Intron			XP_016879971.1
XM_017024483.1	2998	Intron			XP_016879972.1

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