Product Details

SNP ID

rs41289234

Assay Type

Functionally tested

NCBI dbSNP Submissions

23

Location

Chr.1:75130703 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGAGCCCGTATACAGCTCTGCCAT[C/G]TCTGAGGGGTTATGCAGATTCTGAG

Phenotype

MIM: 604425

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

LHX8 PubMed Links

Gene Details

Gene

LHX8

Gene Name

LIM homeobox 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001933.1	653	UTR 5			NP_001001933.1
NM_001256114.1	653	Intron			NP_001243043.1
XM_017001316.1	653	Intron			XP_016856805.1
XM_017001317.1	653	Intron			XP_016856806.1

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