Product Details

SNP ID

rs145981438

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:94455348 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCTTGGGGTTTCCGGCTGCAGGG[C/T]GGTAAGGATTTCAACATGCCTCTGA

Phenotype

MIM: 605904

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PDLIM5 PubMed Links

Gene Details

Gene

PDLIM5

Gene Name

PDZ and LIM domain 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001011513.3	211	Silent Mutation	GGC,GGT	G20G	NP_001011513.3
NM_001011515.2	211	Silent Mutation	GGC,GGT	G20G	NP_001011515.1
NM_001011516.2	211	Silent Mutation	GGC,GGT	G20G	NP_001011516.1
NM_001256425.1	211	UTR 5			NP_001243354.1
NM_001256426.1	211	Silent Mutation	GGC,GGT	G20G	NP_001243355.1
NM_001256427.1	211	Silent Mutation	GGC,GGT	G20G	NP_001243356.1
NM_001256428.1	211	UTR 5			NP_001243357.1
NM_001256429.1	211	Silent Mutation	GGC,GGT	G20G	NP_001243358.1
NM_006457.4	211	Silent Mutation	GGC,GGT	G20G	NP_006448.4
XM_005262693.4	211	Silent Mutation	GGC,GGT	G20G	XP_005262750.1
XM_005262695.4	211	Silent Mutation	GGC,GGT	G20G	XP_005262752.1
XM_005262696.4	211	Silent Mutation	GGC,GGT	G20G	XP_005262753.1
XM_005262698.4	211	Silent Mutation	GGC,GGT	G20G	XP_005262755.1
XM_006714066.3	211	Silent Mutation	GGC,GGT	G20G	XP_006714129.1
XM_006714068.3	211	Silent Mutation	GGC,GGT	G20G	XP_006714131.1
XM_006714069.3	211	Silent Mutation	GGC,GGT	G20G	XP_006714132.1
XM_006714070.3	211	Silent Mutation	GGC,GGT	G20G	XP_006714133.1
XM_011531543.2	211	Silent Mutation	GGC,GGT	G20G	XP_011529845.1
XM_017007657.1	211	Silent Mutation	GGC,GGT	G20G	XP_016863146.1
XM_017007658.1	211	Silent Mutation	GGC,GGT	G20G	XP_016863147.1

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