Product Details

SNP ID
rs115780504
Assay Type
Functionally tested
NCBI dbSNP Submissions
15
Location
Chr.1:226239951 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATTTCTGAGAAAGCACGTTGTTA[C/T]GCACTAAGGAAGCAAAATCGCTCCT
Phenotype
MIM: 609375
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LIN9 PubMed Links

Gene Details

Gene
LIN9
Gene Name
lin-9 DREAM MuvB core complex component
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270409.1 Intron NP_001257338.1
NM_001270410.1 Intron NP_001257339.1
NM_173083.3 Intron NP_775106.2
XM_005273102.3 Intron XP_005273159.1
XM_006711766.2 Intron XP_006711829.2
XM_006711767.3 Intron XP_006711830.1
XM_011544173.2 Intron XP_011542475.1
XM_017001084.1 Intron XP_016856573.1

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