Product Details

SNP ID

rs2039196

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:122187322 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTTTTAATTCTAATTTCAAGACT[A/G]GACTAGAGGTCTGTGGTTTTCTGAT

Phenotype

MIM: 608215

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LHX6 PubMed Links

Gene Details

Gene

LHX6

Gene Name

LIM homeobox 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242333.1		Intron			NP_001229262.1
NM_001242334.1		Intron			NP_001229263.1
NM_001242335.1		Intron			NP_001229264.1
NM_014368.4		Intron			NP_055183.2
NM_199160.3		Intron			NP_954629.2
XM_005251916.3		Intron			XP_005251973.1
XM_011518521.2		Intron			XP_011516823.1
XM_011518522.2		Intron			XP_011516824.1

Gene

MORN5

Gene Name

MORN repeat containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286828.1		Intron			NP_001273757.1
NM_198469.3		Intron			NP_940871.2
XM_005251877.4		Intron			XP_005251934.1
XM_005251878.3		Intron			XP_005251935.1
XM_006717034.3		Intron			XP_006717097.1
XM_011518457.2		Intron			XP_011516759.1
XM_011518458.1		Intron			XP_011516760.1
XM_017014578.1		Intron			XP_016870067.1

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