Product Details

SNP ID

rs2377028

Assay Type

Functionally tested

NCBI dbSNP Submissions

42

Location

Chr.1:226231536 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTACAAGATTAACATTTTAGGCAG[C/G]GTTTTCCTAAAAAAGAAAAACAACC

Phenotype

MIM: 609375 MIM: 609852

Polymorphism

C/G, Transversion 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	2613	UTR 3			NP_001257338.1
NM_001270410.1	2613	UTR 3			NP_001257339.1
NM_173083.3	2613	UTR 3			NP_775106.2
XM_005273102.3	2613	UTR 3			XP_005273159.1
XM_006711766.2	2613	UTR 3			XP_006711829.2
XM_006711767.3	2613	UTR 3			XP_006711830.1
XM_011544173.2	2613	Intron			XP_011542475.1
XM_017001084.1	2613	UTR 3			XP_016856573.1

Gene

MIXL1

Gene Name

Mix paired-like homeobox

There are no transcripts associated with this gene.

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