Product Details

SNP ID
rs200137561
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:32222308 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAAGGGCGGGGCCGGCTACCTACC[A/C]AGAGACGCCGCCATGGCAACGCCGC
Phenotype
MIM: 603911
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
DCDC2B PubMed Links

Gene Details

Gene
DCDC2B
Gene Name
doublecortin domain containing 2B
There are no transcripts associated with this gene.

Gene
EIF3I
Gene Name
eukaryotic translation initiation factor 3 subunit I
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003757.3 46 Intron NP_003748.1
XM_017002671.1 46 Intron XP_016858160.1
Gene
MTMR9LP
Gene Name
myotubularin related protein 9-like, pseudogene
There are no transcripts associated with this gene.

Gene
TMEM234
Gene Name
transmembrane protein 234
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_019118.4 46 Silent Mutation CTG,CTT L5L NP_061991.3
XM_011541795.2 46 Silent Mutation CTG,CTT L5L XP_011540097.1
XM_017001812.1 46 Silent Mutation CTG,CTT L5L XP_016857301.1
XM_017001813.1 46 Silent Mutation CTG,CTT L5L XP_016857302.1
XM_017001814.1 46 Silent Mutation CTG,CTT L5L XP_016857303.1
XM_017001815.1 46 Silent Mutation CTG,CTT L5L XP_016857304.1
XM_017001816.1 46 Silent Mutation CTG,CTT L5L XP_016857305.1
XM_017001817.1 46 Silent Mutation CTG,CTT L5L XP_016857306.1
XM_017001818.1 46 Silent Mutation CTG,CTT L5L XP_016857307.1
XM_017001819.1 46 Silent Mutation CTG,CTT L5L XP_016857308.1
XM_017001820.1 46 Silent Mutation CTG,CTT L5L XP_016857309.1
XM_017001821.1 46 Silent Mutation CTG,CTT L5L XP_016857310.1
XM_017001822.1 46 Silent Mutation CTG,CTT L5L XP_016857311.1
XM_017001823.1 46 Silent Mutation CTG,CTT L5L XP_016857312.1
XM_017001824.1 46 Silent Mutation CTG,CTT L5L XP_016857313.1
XM_017001825.1 46 Silent Mutation CTG,CTT L5L XP_016857314.1
XM_017001826.1 46 Silent Mutation CTG,CTT L5L XP_016857315.1
XM_017001827.1 46 Silent Mutation CTG,CTT L5L XP_016857316.1
XM_017001828.1 46 Silent Mutation CTG,CTT L5L XP_016857317.1
XM_017001829.1 46 Silent Mutation CTG,CTT L5L XP_016857318.1
XM_017001830.1 46 Silent Mutation CTG,CTT L5L XP_016857319.1
XM_017001831.1 46 UTR 5 XP_016857320.1

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