Product Details

SNP ID
rs199926651
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.14:22902076 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGCGGCAGCAGCAGCAGCAGCAG[C/T]GCTTGGCAGTTGGATTCCAGCGCCT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
RBM23 PubMed Links

Gene Details

Gene
RBM23
Gene Name
RNA binding motif protein 23
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001077351.1 1333 Missense Mutation ACT,GCT T384A NP_001070819.1
NM_001077352.1 1333 Missense Mutation ACT,GCT T350A NP_001070820.1
NM_001308044.1 1333 Missense Mutation ACT,GCT T214A NP_001294973.1
NM_018107.4 1333 Missense Mutation ACT,GCT T368A NP_060577.3
XM_011536890.2 1333 Missense Mutation ACT,GCT T428A XP_011535192.1
XM_011536892.2 1333 Missense Mutation ACT,GCT T412A XP_011535194.1
XM_011536893.2 1333 Missense Mutation ACT,GCT T412A XP_011535195.1
XM_011536894.2 1333 Missense Mutation ACT,GCT T410A XP_011535196.1
XM_011536895.2 1333 Missense Mutation ACT,GCT T394A XP_011535197.1
XM_011536896.2 1333 Missense Mutation ACT,GCT T394A XP_011535198.1
XM_011536897.2 1333 Missense Mutation ACT,GCT T386A XP_011535199.1
XM_011536900.1 1333 Missense Mutation ACT,GCT T366A XP_011535202.1
XM_011536902.1 1333 Missense Mutation ACT,GCT T214A XP_011535204.1
XM_011536903.1 1333 Missense Mutation ACT,GCT T214A XP_011535205.1
XM_011536904.1 1333 Missense Mutation ACT,GCT T214A XP_011535206.1
XM_011536905.1 1333 Missense Mutation ACT,GCT T214A XP_011535207.1
XM_011536906.1 1333 Missense Mutation ACT,GCT T214A XP_011535208.1
XM_017021398.1 1333 Missense Mutation ACT,GCT T412A XP_016876887.1
XM_017021399.1 1333 Missense Mutation ACT,GCT T394A XP_016876888.1
XM_017021400.1 1333 Missense Mutation ACT,GCT T386A XP_016876889.1
XM_017021401.1 1333 Missense Mutation ACT,GCT T384A XP_016876890.1
XM_017021402.1 1333 Missense Mutation ACT,GCT T384A XP_016876891.1
XM_017021403.1 1333 Missense Mutation ACT,GCT T368A XP_016876892.1
XM_017021404.1 1333 Missense Mutation ACT,GCT T368A XP_016876893.1
XM_017021405.1 1333 Missense Mutation ACT,GCT T366A XP_016876894.1
XM_017021406.1 1333 Missense Mutation ACT,GCT T402A XP_016876895.1
XM_017021407.1 1333 Missense Mutation ACT,GCT T384A XP_016876896.1
XM_017021408.1 1333 Missense Mutation ACT,GCT T350A XP_016876897.1
XM_017021409.1 1333 Missense Mutation ACT,GCT T384A XP_016876898.1
XM_017021410.1 1333 Missense Mutation ACT,GCT T350A XP_016876899.1
XM_017021411.1 1333 Missense Mutation ACT,GCT T368A XP_016876900.1
XM_017021412.1 1333 Intron XP_016876901.1
XM_017021413.1 1333 Intron XP_016876902.1
XM_017021414.1 1333 Missense Mutation ACT,GCT T214A XP_016876903.1
XM_017021415.1 1333 Missense Mutation ACT,GCT T214A XP_016876904.1
XM_017021416.1 1333 Missense Mutation ACT,GCT T214A XP_016876905.1
XM_017021417.1 1333 Missense Mutation ACT,GCT T214A XP_016876906.1
XM_017021418.1 1333 Missense Mutation ACT,GCT T214A XP_016876907.1
XM_017021419.1 1333 Missense Mutation ACT,GCT T214A XP_016876908.1
XM_017021420.1 1333 Missense Mutation ACT,GCT T214A XP_016876909.1

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