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AGTCAGAGCTGCTGGATTCAGGGCC[C/T]CCAAGGGAACTGCTCCATTCAGTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
RBM23 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
RBM23 - RNA binding motif protein 23 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077351.1 | 1403 | Missense Mutation | GAG,GGG | E,G 407 | NP_001070819.1 | |
NM_001077352.1 | 1403 | Missense Mutation | GAG,GGG | E,G 373 | NP_001070820.1 | |
NM_001308044.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | NP_001294973.1 | |
NM_018107.4 | 1403 | Missense Mutation | GAG,GGG | E,G 391 | NP_060577.3 | |
XM_011536890.2 | 1403 | Missense Mutation | GAG,GGG | E,G 451 | XP_011535192.1 | |
XM_011536892.2 | 1403 | Missense Mutation | GAG,GGG | E,G 435 | XP_011535194.1 | |
XM_011536893.2 | 1403 | Missense Mutation | GAG,GGG | E,G 435 | XP_011535195.1 | |
XM_011536894.2 | 1403 | Missense Mutation | GAG,GGG | E,G 433 | XP_011535196.1 | |
XM_011536895.2 | 1403 | Missense Mutation | GAG,GGG | E,G 417 | XP_011535197.1 | |
XM_011536896.2 | 1403 | Missense Mutation | GAG,GGG | E,G 417 | XP_011535198.1 | |
XM_011536897.2 | 1403 | Missense Mutation | GAG,GGG | E,G 409 | XP_011535199.1 | |
XM_011536900.1 | 1403 | Missense Mutation | GAG,GGG | E,G 389 | XP_011535202.1 | |
XM_011536902.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_011535204.1 | |
XM_011536903.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_011535205.1 | |
XM_011536904.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_011535206.1 | |
XM_011536905.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_011535207.1 | |
XM_011536906.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_011535208.1 | |
XM_017021398.1 | 1403 | Missense Mutation | GAG,GGG | E,G 435 | XP_016876887.1 | |
XM_017021399.1 | 1403 | Missense Mutation | GAG,GGG | E,G 417 | XP_016876888.1 | |
XM_017021400.1 | 1403 | Missense Mutation | GAG,GGG | E,G 409 | XP_016876889.1 | |
XM_017021401.1 | 1403 | Missense Mutation | GAG,GGG | E,G 407 | XP_016876890.1 | |
XM_017021402.1 | 1403 | Missense Mutation | GAG,GGG | E,G 407 | XP_016876891.1 | |
XM_017021403.1 | 1403 | Missense Mutation | GAG,GGG | E,G 391 | XP_016876892.1 | |
XM_017021404.1 | 1403 | Missense Mutation | GAG,GGG | E,G 391 | XP_016876893.1 | |
XM_017021405.1 | 1403 | Missense Mutation | GAG,GGG | E,G 389 | XP_016876894.1 | |
XM_017021406.1 | 1403 | Missense Mutation | GAG,GGG | E,G 425 | XP_016876895.1 | |
XM_017021407.1 | 1403 | Missense Mutation | GAG,GGG | E,G 407 | XP_016876896.1 | |
XM_017021408.1 | 1403 | Missense Mutation | GAG,GGG | E,G 373 | XP_016876897.1 | |
XM_017021409.1 | 1403 | Missense Mutation | GAG,GGG | E,G 407 | XP_016876898.1 | |
XM_017021410.1 | 1403 | Missense Mutation | GAG,GGG | E,G 373 | XP_016876899.1 | |
XM_017021411.1 | 1403 | Missense Mutation | GAG,GGG | E,G 391 | XP_016876900.1 | |
XM_017021412.1 | 1403 | Intron | XP_016876901.1 | |||
XM_017021413.1 | 1403 | Intron | XP_016876902.1 | |||
XM_017021414.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876903.1 | |
XM_017021415.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876904.1 | |
XM_017021416.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876905.1 | |
XM_017021417.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876906.1 | |
XM_017021418.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876907.1 | |
XM_017021419.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876908.1 | |
XM_017021420.1 | 1403 | Missense Mutation | GAG,GGG | E,G 237 | XP_016876909.1 |