Product Details

SNP ID
rs112462767
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:307312 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAGGGGCAGCTCCTTGGGCAGGG[C/T]GAAGTCCACGGCCAGCCTTGGGCTG
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 2016 Missense Mutation ACC,GCC T477A XP_005259639.1
XM_006722769.3 2016 Missense Mutation ACC,GCC T470A XP_006722832.1
XM_011528072.2 2016 Missense Mutation ACC,GCC T477A XP_011526374.1
XM_011528073.1 2016 Missense Mutation ACC,GCC T475A XP_011526375.1
XM_011528074.2 2016 Missense Mutation ACC,GCC T470A XP_011526376.1
XM_011528075.2 2016 Missense Mutation ACC,GCC T439A XP_011526377.1
XM_011528077.2 2016 Missense Mutation ACC,GCC T439A XP_011526379.1
XM_011528081.2 2016 Missense Mutation ACC,GCC T399A XP_011526383.1
XM_011528082.2 2016 Missense Mutation ACC,GCC T391A XP_011526384.1

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