Product Details

SNP ID

rs151275498

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:226225738 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTCAGAATTTTGAAACCTGTTCC[C/T]CTCTCTCTGAAGACATTGGTTCAAA

Phenotype

MIM: 609375 MIM: 609852

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

There are no transcripts associated with this gene.

Gene

MIXL1

Gene Name

Mix paired-like homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282402.1	713	Missense Mutation	CCT,TCT	P217S	NP_001269331.1
NM_031944.2	713	Missense Mutation	CCT,TCT	P209S	NP_114150.1

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