Product Details

SNP ID
rs816723
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.5:154868854 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GGCTGTGGCTTCCTTGGCCTGGACC[A/G]CTTCCTCCCTCTGCAGGTGGTACTG
Phenotype
MIM: 603731
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CNOT8 PubMed Links

Gene Details

Gene
CNOT8
Gene Name
CCR4-NOT transcription complex subunit 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001301073.1 Intron NP_001288002.1
NM_001301074.1 Intron NP_001288003.1
NM_001301075.1 Intron NP_001288004.1
NM_001301077.1 Intron NP_001288006.1
NM_001301080.1 Intron NP_001288009.1
NM_001301082.1 Intron NP_001288011.1
NM_001301083.1 Intron NP_001288012.1
NM_001301086.1 Intron NP_001288015.1
NM_004779.5 Intron NP_004770.4
XM_005268527.2 Intron XP_005268584.1
XM_011537706.1 Intron XP_011536008.1
XM_011537708.2 Intron XP_011536010.1
XM_017010048.1 Intron XP_016865537.1
XM_017010049.1 Intron XP_016865538.1
XM_017010050.1 Intron XP_016865539.1
XM_017010051.1 Intron XP_016865540.1
XM_017010052.1 Intron XP_016865541.1
XM_017010053.1 Intron XP_016865542.1
XM_017010054.1 Intron XP_016865543.1
XM_017010055.1 Intron XP_016865544.1
XM_017010056.1 Intron XP_016865545.1
XM_017010057.1 Intron XP_016865546.1
XM_017010058.1 Intron XP_016865547.1

View Full Product Details