Product Details

SNP ID

rs76242063

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:16502661 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCATCTTATTGGGAAGCCTGGGG[C/T]GGGGGGTTTTCTGATTTGGTCTCTT

Phenotype

MIM: 603450

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LDB2 PubMed Links

Gene Details

Gene

LDB2

Gene Name

LIM domain binding 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130834.2	1859	UTR 3			NP_001124306.1
NM_001290.4	1859	Silent Mutation	CCA,CCG	P368P	NP_001281.1
NM_001304434.1	1859	Silent Mutation	CCA,CCG	P366P	NP_001291363.1
NM_001304435.1	1859	UTR 3			NP_001291364.1
XM_005248197.3	1859	Silent Mutation	CCA,CCG	P367P	XP_005248254.1
XM_005248201.2	1859	UTR 3			XP_005248258.1
XM_005248202.2	1859	UTR 3			XP_005248259.1
XM_006713975.3	1859	Silent Mutation	CCA,CCG	P406P	XP_006714038.1
XM_006713976.3	1859	Silent Mutation	CCA,CCG	P405P	XP_006714039.1
XM_006713977.3	1859	Silent Mutation	CCA,CCG	P404P	XP_006714040.1
XM_006713978.3	1859	UTR 3			XP_006714041.1
XM_006713979.3	1859	UTR 3			XP_006714042.1
XM_006713980.3	1859	UTR 3			XP_006714043.1
XM_006713981.3	1859	UTR 3			XP_006714044.1
XM_006713982.3	1859	UTR 3			XP_006714045.1
XM_006713983.3	1859	UTR 3			XP_006714046.1
XM_011513905.2	1859	Silent Mutation	CCA,CCG	P293P	XP_011512207.1
XM_017008812.1	1859	Silent Mutation	CCA,CCG	P403P	XP_016864301.1
XM_017008813.1	1859	Silent Mutation	CCA,CCG	P365P	XP_016864302.1
XM_017008814.1	1859	UTR 3			XP_016864303.1
XM_017008815.1	1859	UTR 3			XP_016864304.1
XM_017008816.1	1859	UTR 3			XP_016864305.1
XM_017008817.1	1859	UTR 3			XP_016864306.1
XM_017008818.1	1859	Silent Mutation	CCA,CCG	P325P	XP_016864307.1
XM_017008819.1	1859	UTR 3			XP_016864308.1
XM_017008820.1	1859	UTR 3			XP_016864309.1
XM_017008821.1	1859	UTR 3			XP_016864310.1
XM_017008822.1	1859	Silent Mutation	CCA,CCG	P244P	XP_016864311.1

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