Product Details

SNP ID

rs113279920

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:121810045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCACTGGGGGCAGCAGCGGTCCCC[C/T]GTTCAAGGCTCAACCACAGGATTCA

Phenotype

MIM: 611055

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LINC01089 PubMed Links

Gene Details

Gene

LINC01089

Gene Name

long intergenic non-protein coding RNA 1089

There are no transcripts associated with this gene.

Gene

SETD1B

Gene Name

SET domain containing 1B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015048.1	1265	Missense Mutation	CCG,CTG	P367L	NP_055863.1
XM_005253858.4	1265	Missense Mutation	CCG,CTG	P367L	XP_005253915.1
XM_006719296.3	1265	Missense Mutation	CCG,CTG	P367L	XP_006719359.1

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