Product Details

SNP ID
rs148255294
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:22901824 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCCTGAGACTCACATGGTCTGGG[A/G]GGTAAAGAGGCTGGAGAGCTGGAAA
Phenotype
Polymorphism
A/G, 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 1585 Missense Mutation CCC,TCC P436S NP_001070819.1
NM_001077352.1 1585 Missense Mutation CCC,TCC P402S NP_001070820.1
NM_001308044.1 1585 Missense Mutation CCC,TCC P266S NP_001294973.1
NM_018107.4 1585 Missense Mutation CCC,TCC P420S NP_060577.3
XM_011536890.2 1585 Missense Mutation CCC,TCC P480S XP_011535192.1
XM_011536892.2 1585 Missense Mutation CCC,TCC P464S XP_011535194.1
XM_011536893.2 1585 Missense Mutation CCC,TCC P464S XP_011535195.1
XM_011536894.2 1585 Missense Mutation CCC,TCC P462S XP_011535196.1
XM_011536895.2 1585 Missense Mutation CCC,TCC P446S XP_011535197.1
XM_011536896.2 1585 Missense Mutation CCC,TCC P446S XP_011535198.1
XM_011536897.2 1585 Missense Mutation CCC,TCC P438S XP_011535199.1
XM_011536900.1 1585 Missense Mutation CCC,TCC P418S XP_011535202.1
XM_011536902.1 1585 Missense Mutation CCC,TCC P266S XP_011535204.1
XM_011536903.1 1585 Missense Mutation CCC,TCC P266S XP_011535205.1
XM_011536904.1 1585 Missense Mutation CCC,TCC P266S XP_011535206.1
XM_011536905.1 1585 Missense Mutation CCC,TCC P266S XP_011535207.1
XM_011536906.1 1585 Missense Mutation CCC,TCC P266S XP_011535208.1
XM_017021398.1 1585 Missense Mutation CCC,TCC P496S XP_016876887.1
XM_017021399.1 1585 Missense Mutation CCC,TCC P478S XP_016876888.1
XM_017021400.1 1585 Missense Mutation CCC,TCC P470S XP_016876889.1
XM_017021401.1 1585 Missense Mutation CCC,TCC P468S XP_016876890.1
XM_017021402.1 1585 Missense Mutation CCC,TCC P468S XP_016876891.1
XM_017021403.1 1585 Missense Mutation CCC,TCC P452S XP_016876892.1
XM_017021404.1 1585 Missense Mutation CCC,TCC P452S XP_016876893.1
XM_017021405.1 1585 Missense Mutation CCC,TCC P450S XP_016876894.1
XM_017021406.1 1585 Missense Mutation CCC,TCC P454S XP_016876895.1
XM_017021407.1 1585 Missense Mutation CCC,TCC P436S XP_016876896.1
XM_017021408.1 1585 Missense Mutation CCC,TCC P434S XP_016876897.1
XM_017021409.1 1585 Missense Mutation CCC,TCC P436S XP_016876898.1
XM_017021410.1 1585 Missense Mutation CCC,TCC P402S XP_016876899.1
XM_017021411.1 1585 Missense Mutation CCC,TCC P420S XP_016876900.1
XM_017021412.1 1585 Intron XP_016876901.1
XM_017021413.1 1585 Intron XP_016876902.1
XM_017021414.1 1585 Missense Mutation CCC,TCC P298S XP_016876903.1
XM_017021415.1 1585 Missense Mutation CCC,TCC P298S XP_016876904.1
XM_017021416.1 1585 Missense Mutation CCC,TCC P298S XP_016876905.1
XM_017021417.1 1585 Missense Mutation CCC,TCC P298S XP_016876906.1
XM_017021418.1 1585 Missense Mutation CCC,TCC P298S XP_016876907.1
XM_017021419.1 1585 Missense Mutation CCC,TCC P298S XP_016876908.1
XM_017021420.1 1585 Missense Mutation CCC,TCC P266S XP_016876909.1

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