Product Details

SNP ID

rs202211730

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:5692978 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGATCTCCAAGAGGCTGGGCAAGC[G/T]CTGGAAAATGCTGAAGGACAGCGAG

Phenotype

MIM: 600898

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LINC01248 PubMed Links

Gene Details

Gene

LINC01248

Gene Name

long intergenic non-protein coding RNA 1248

There are no transcripts associated with this gene.

Gene

SOX11

Gene Name

SRY-box 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003108.3	312	Missense Mutation	CGC,CTC	R86L	NP_003099.1

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