Product Details

SNP ID

rs202197852

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:61947011 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCACTGAAGGCACGTGGAGGTGCA[A/G]AGAGGCCTAAGAAGGTAACAGGTAA

Phenotype

MIM: 603808

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MED13 PubMed Links

Gene Details

Gene

MED13

Gene Name

mediator complex subunit 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005121.2	5790	Silent Mutation	CTG,TTG	L2100L	NP_005112.2
XM_011525551.2	5790	Silent Mutation	CTG,TTG	L2047L	XP_011523853.1
XM_011525552.2	5790	Intron			XP_011523854.1
XM_011525553.2	5790	Silent Mutation	CTG,TTG	L1877L	XP_011523855.1

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