Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTGTGAGGCGCTGGGCCCGGAAA[C/T]GGGGAGGGCGGGCCACCCACACACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609066 | ||||||||||||||||||||
Literature Links: |
AJUBA PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
AJUBA - ajuba LIM protein | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
C14orf93 - chromosome 14 open reading frame 93 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130706.2 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | NP_001124178.1 | |
NM_001130708.2 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | NP_001124180.1 | |
NM_001282968.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | NP_001269897.1 | |
NM_001282969.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | NP_001269898.1 | |
NM_001282970.1 | 1516 | Intron | NP_001269899.1 | |||
NM_021944.3 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | NP_068763.2 | |
XM_005267971.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_005268028.1 | |
XM_005267972.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_005268029.1 | |
XM_006720231.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | XP_006720294.1 | |
XM_006720232.2 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | XP_006720295.1 | |
XM_011537059.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_011535361.1 | |
XM_011537060.2 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_011535362.1 | |
XM_011537062.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_011535364.1 | |
XM_017021569.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877058.1 | |
XM_017021570.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877059.1 | |
XM_017021571.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877060.1 | |
XM_017021572.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877061.1 | |
XM_017021573.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877062.1 | |
XM_017021574.1 | 1516 | Missense Mutation | CAT,CGT | H,R 446 | XP_016877063.1 | |
XM_017021575.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | XP_016877064.1 | |
XM_017021576.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | XP_016877065.1 | |
XM_017021577.1 | 1516 | Missense Mutation | CAT,CGT | H,R 266 | XP_016877066.1 |