Product Details

SNP ID

rs12141189

Assay Type

Functionally tested

NCBI dbSNP Submissions

36

Location

Chr.1:220880203 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTCCCGCAGCGGCTGTCTCCGCTC[C/T]CAGCCGCCTACCACCACCATCACCC

Phenotype

MIM: 142995

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HLX PubMed Links

Gene Details

Gene

HLX

Gene Name

H2.0 like homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021958.3	803	Missense Mutation	CCA,TCA	P116S	NP_068777.1

Gene

HLX-AS1

Gene Name

HLX antisense RNA 1

There are no transcripts associated with this gene.

View Full Product Details