Product Details

SNP ID
rs140382721
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:226233128 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGAAGCGTCTATTGTACTCTTGAT[A/G]TCATTTAATGAGTCTGTAAGTGATT
Phenotype
MIM: 609375 MIM: 609852
Polymorphism
A/G, 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 1510 Silent Mutation GAC,GAT D478D NP_001257338.1
NM_001270410.1 1510 Silent Mutation GAC,GAT D445D NP_001257339.1
NM_173083.3 1510 Silent Mutation GAC,GAT D513D NP_775106.2
XM_005273102.3 1510 Silent Mutation GAC,GAT D570D XP_005273159.1
XM_006711766.2 1510 Silent Mutation GAC,GAT D479D XP_006711829.2
XM_006711767.3 1510 Silent Mutation GAC,GAT D445D XP_006711830.1
XM_011544173.2 1510 Intron XP_011542475.1
XM_017001084.1 1510 Silent Mutation GAC,GAT D501D XP_016856573.1
Gene
MIXL1
Gene Name
Mix paired-like homeobox
There are no transcripts associated with this gene.

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