Product Details

SNP ID
rs1127678
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:82101611 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCTGTGCCCACACCCCCCCACAACA[C/T]GTAGGTGAAAGCACAGGCACCATGC
Phenotype
MIM: 600212
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 3065 Intron NP_001303250.1
NM_198082.2 3065 UTR 3 NP_932348.2
XM_011523545.2 3065 Intron XP_011521847.2
XM_011523546.2 3065 Intron XP_011521848.1
XM_011523548.2 3065 Intron XP_011521850.1
XM_011523549.2 3065 Intron XP_011521851.1
XM_011523551.2 3065 Intron XP_011521853.1
XM_011523552.2 3065 Intron XP_011521854.1
XM_011523555.2 3065 Intron XP_011521857.1
XM_011523556.2 3065 Intron XP_011521858.2
XM_011523557.2 3065 Intron XP_011521859.1
XM_017024462.1 3065 Intron XP_016879951.1
XM_017024463.1 3065 UTR 3 XP_016879952.1
XM_017024464.1 3065 Intron XP_016879953.1
XM_017024465.1 3065 Intron XP_016879954.1
XM_017024466.1 3065 UTR 3 XP_016879955.1
XM_017024467.1 3065 Intron XP_016879956.1
XM_017024468.1 3065 Intron XP_016879957.1
XM_017024469.1 3065 Intron XP_016879958.1
XM_017024470.1 3065 Intron XP_016879959.1
XM_017024471.1 3065 Intron XP_016879960.1
XM_017024472.1 3065 Intron XP_016879961.1
XM_017024473.1 3065 Intron XP_016879962.1
XM_017024474.1 3065 Intron XP_016879963.1
XM_017024475.1 3065 Intron XP_016879964.1
XM_017024476.1 3065 Intron XP_016879965.1
XM_017024477.1 3065 Intron XP_016879966.1
XM_017024478.1 3065 Intron XP_016879967.1
XM_017024479.1 3065 UTR 3 XP_016879968.1
XM_017024480.1 3065 Intron XP_016879969.1
XM_017024481.1 3065 Intron XP_016879970.1
XM_017024482.1 3065 Intron XP_016879971.1
XM_017024483.1 3065 UTR 3 XP_016879972.1
Gene
FASN
Gene Name
fatty acid synthase
There are no transcripts associated with this gene.

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