Product Details

SNP ID

rs113219038

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:115963511 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGTGCTACTGAAATGTGGTGATG[C/T]AGCGAAGCCTGGTGAAAAAACAAAG

Phenotype

MIM: 608771

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MED13L PubMed Links

Gene Details

Gene

MED13L

Gene Name

mediator complex subunit 13 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015335.4	6451	Silent Mutation	CTA,CTG	L2132L	NP_056150.1
XM_011538080.2	6451	Silent Mutation	CTA,CTG	L2144L	XP_011536382.1
XM_011538081.2	6451	Silent Mutation	CTA,CTG	L2143L	XP_011536383.1
XM_011538082.2	6451	Silent Mutation	CTA,CTG	L2134L	XP_011536384.1
XM_017019090.1	6451	Silent Mutation	CTA,CTG	L2131L	XP_016874579.1

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