Product Details

SNP ID
rs35042658
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:307282 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATCCCCGCTGAGGTCCACATGGC[T/C]GGAGATGAGGGGCAGCTCCTTGGGC
Phenotype
Polymorphism
T/C, 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 2046 Missense Mutation AGC,GGC S487G XP_005259639.1
XM_006722769.3 2046 Missense Mutation AGC,GGC S480G XP_006722832.1
XM_011528072.2 2046 Missense Mutation AGC,GGC S487G XP_011526374.1
XM_011528073.1 2046 Missense Mutation AGC,GGC S485G XP_011526375.1
XM_011528074.2 2046 Missense Mutation AGC,GGC S480G XP_011526376.1
XM_011528075.2 2046 Missense Mutation AGC,GGC S449G XP_011526377.1
XM_011528077.2 2046 Missense Mutation AGC,GGC S449G XP_011526379.1
XM_011528081.2 2046 Missense Mutation AGC,GGC S409G XP_011526383.1
XM_011528082.2 2046 Missense Mutation AGC,GGC S401G XP_011526384.1

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