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Search Thermo Fisher Scientific
AAGGGCGGGGCCGGCTACCTACCCA[C/G]AGACGCCGCCATGGCAACGCCGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 603911 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DCDC2B 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DCDC2B - doublecortin domain containing 2B | ||||||
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There are no transcripts associated with this gene. |
EIF3I - eukaryotic translation initiation factor 3 subunit I | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003757.3 | 44 | Intron | NP_003748.1 | |||
XM_017002671.1 | 44 | Intron | XP_016858160.1 |
MTMR9LP - myotubularin related protein 9-like, pseudogene | ||||||
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There are no transcripts associated with this gene. |
TMEM234 - transmembrane protein 234 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019118.4 | 44 | Missense Mutation | CTG,GTG | L,V 5 | NP_061991.3 | |
XM_011541795.2 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_011540097.1 | |
XM_017001812.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857301.1 | |
XM_017001813.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857302.1 | |
XM_017001814.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857303.1 | |
XM_017001815.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857304.1 | |
XM_017001816.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857305.1 | |
XM_017001817.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857306.1 | |
XM_017001818.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857307.1 | |
XM_017001819.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857308.1 | |
XM_017001820.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857309.1 | |
XM_017001821.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857310.1 | |
XM_017001822.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857311.1 | |
XM_017001823.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857312.1 | |
XM_017001824.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857313.1 | |
XM_017001825.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857314.1 | |
XM_017001826.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857315.1 | |
XM_017001827.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857316.1 | |
XM_017001828.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857317.1 | |
XM_017001829.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857318.1 | |
XM_017001830.1 | 44 | Missense Mutation | CTG,GTG | L,V 5 | XP_016857319.1 | |
XM_017001831.1 | 44 | UTR 5 | XP_016857320.1 |