Product Details

SNP ID

rs148132163

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:307515 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCGGGCTCATCGAGACCACCGGCC[A/G]TGCCATCCACGCTCAGTGGATCTGT

Phenotype

Polymorphism

A/G, 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	1813	Missense Mutation	ACG,ATG	T409M	XP_005259639.1
XM_006722769.3	1813	Missense Mutation	ACG,ATG	T402M	XP_006722832.1
XM_011528072.2	1813	Missense Mutation	ACG,ATG	T409M	XP_011526374.1
XM_011528073.1	1813	Missense Mutation	ACG,ATG	T407M	XP_011526375.1
XM_011528074.2	1813	Missense Mutation	ACG,ATG	T402M	XP_011526376.1
XM_011528075.2	1813	Missense Mutation	ACG,ATG	T371M	XP_011526377.1
XM_011528077.2	1813	Missense Mutation	ACG,ATG	T371M	XP_011526379.1
XM_011528081.2	1813	Missense Mutation	ACG,ATG	T331M	XP_011526383.1
XM_011528082.2	1813	Missense Mutation	ACG,ATG	T323M	XP_011526384.1

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