Product Details

SNP ID
rs151055354
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:36892433 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTCCCATAGGACCACCCTGAGAAA[C/T]GTAGTCCCCTGGCATGCTCTGCAAA
Phenotype
MIM: 601740
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LOC145845 PubMed Links

Gene Details

Gene
LOC145845
Gene Name
uncharacterized LOC145845
There are no transcripts associated with this gene.

Gene
MEIS2
Gene Name
Meis homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001220482.1 1694 Missense Mutation ATT,GTT I385V NP_001207411.1
NM_002399.3 1694 UTR 3 NP_002390.1
NM_170674.4 1694 UTR 3 NP_733774.1
NM_170675.4 1694 Missense Mutation ATT,GTT I392V NP_733775.1
NM_170676.4 1694 Missense Mutation ATT,GTT I385V NP_733776.1
NM_170677.4 1694 UTR 3 NP_733777.1
NM_172315.2 1694 UTR 3 NP_758526.1
NM_172316.2 1694 UTR 3 NP_758527.1
XM_006720523.1 1694 Missense Mutation ATT,GTT I391V XP_006720586.1
XM_006720524.1 1694 UTR 3 XP_006720587.1
XM_006720525.1 1694 UTR 3 XP_006720588.1
XM_006720526.2 1694 Missense Mutation ATT,GTT I304V XP_006720589.1
XM_006720527.2 1694 Missense Mutation ATT,GTT I246V XP_006720590.1
XM_006720529.2 1694 UTR 3 XP_006720592.1
XM_011521591.2 1694 Missense Mutation ATT,GTT I246V XP_011519893.1
XM_017022205.1 1694 UTR 3 XP_016877694.1

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