Product Details

SNP ID
rs148728346
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:51450161 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTACCTTCTGCTGAACCTGTGGTAA[A/C]ATATTCCTCATAGGGATCCAAGGCC
Phenotype
MIM: 612186
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
DMXL2 PubMed Links

Gene Details

Gene
DMXL2
Gene Name
Dmx like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001174116.1 9220 Missense Mutation GTT,TTT V2958F NP_001167587.1
NM_001174117.1 9220 Missense Mutation GTT,TTT V2321F NP_001167588.1
NM_015263.3 9220 Missense Mutation GTT,TTT V2957F NP_056078.2
XM_005254255.1 9220 Missense Mutation GTT,TTT V2979F XP_005254312.1
XM_005254256.1 9220 Missense Mutation GTT,TTT V2978F XP_005254313.1
XM_011521402.2 9220 Intron XP_011519704.1
XM_017022034.1 9220 Missense Mutation GTT,TTT V2961F XP_016877523.1

View Full Product Details