Product Details

SNP ID

rs140839810

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:307276 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCCGGATCCCCGCTGAGGTCCA[C/T]ATGGCTGGAGATGAGGGGCAGCTCC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC101929060 PubMed Links

Gene Details

Gene

LOC101929060

Gene Name

uncharacterized LOC101929060

There are no transcripts associated with this gene.

Gene

MIER2

Gene Name

MIER family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005259582.4	2052	Missense Mutation	ATG,GTG	M489V	XP_005259639.1
XM_006722769.3	2052	Missense Mutation	ATG,GTG	M482V	XP_006722832.1
XM_011528072.2	2052	Missense Mutation	ATG,GTG	M489V	XP_011526374.1
XM_011528073.1	2052	Missense Mutation	ATG,GTG	M487V	XP_011526375.1
XM_011528074.2	2052	Missense Mutation	ATG,GTG	M482V	XP_011526376.1
XM_011528075.2	2052	Missense Mutation	ATG,GTG	M451V	XP_011526377.1
XM_011528077.2	2052	Missense Mutation	ATG,GTG	M451V	XP_011526379.1
XM_011528081.2	2052	Missense Mutation	ATG,GTG	M411V	XP_011526383.1
XM_011528082.2	2052	Missense Mutation	ATG,GTG	M403V	XP_011526384.1

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