Product Details

SNP ID

rs142967828

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:115961329 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCACCACAAAGTGGACGGGAAGGCA[A/G]GAAGTACGGTCCTGGGTGGCCGGAT

Phenotype

MIM: 608771

Polymorphism

A/G, 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	6625	Silent Mutation	TCC,TCT	S2190S	NP_056150.1
XM_011538080.2	6625	Silent Mutation	TCC,TCT	S2202S	XP_011536382.1
XM_011538081.2	6625	Silent Mutation	TCC,TCT	S2201S	XP_011536383.1
XM_011538082.2	6625	Silent Mutation	TCC,TCT	S2192S	XP_011536384.1
XM_017019090.1	6625	Silent Mutation	TCC,TCT	S2189S	XP_016874579.1

View Full Product Details