Product Details

SNP ID

rs12132601

Assay Type

Functionally tested

NCBI dbSNP Submissions

38

Location

Chr.1:75205530 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACACATGACTATCAGAAACCTCAGG[C/T]GGCCAGCGGTGGCAGGTGGCAACAA

Phenotype

MIM: 604425

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LHX8 PubMed Links

Gene Details

Gene

LHX8

Gene Name

LIM homeobox 8

There are no transcripts associated with this gene.

Gene

SLC44A5

Gene Name

solute carrier family 44 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130058.1	3359	Intron			NP_001123530.1
NM_001320283.1	3359	Intron			NP_001307212.1
NM_001320285.1	3359	Intron			NP_001307214.1
NM_001320287.1	3359	Intron			NP_001307216.1
NM_152697.4	3359	Intron			NP_689910.2
XM_006710445.3	3359	UTR 3			XP_006710508.1
XM_011540986.2	3359	UTR 3			XP_011539288.1
XM_011540987.2	3359	UTR 3			XP_011539289.1
XM_017000607.1	3359	UTR 3			XP_016856096.1
XM_017000608.1	3359	Intron			XP_016856097.1
XM_017000609.1	3359	UTR 3			XP_016856098.1
XM_017000610.1	3359	UTR 3			XP_016856099.1
XM_017000611.1	3359	UTR 3			XP_016856100.1

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