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TGCCCCCACCCAACTGCACCTGTTG[A/G]TGATGATCCGCTGGACGATGAGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614534 MIM: 607996 MIM: 602679 MIM: 606212 | ||||||||||||||||||||
Literature Links: |
ANAPC11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
ANAPC11 - anaphase promoting complex subunit 11 | ||||||
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There are no transcripts associated with this gene. |
NPB - neuropeptide B | ||||||
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There are no transcripts associated with this gene. |
PCYT2 - phosphate cytidylyltransferase 2, ethanolamine | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184917.2 | 1458 | Missense Mutation | ACC,ATC | T,I 369 | NP_001171846.1 | |
NM_001256433.2 | 1458 | Missense Mutation | ACC,ATC | T,I 297 | NP_001243362.1 | |
NM_001256434.2 | 1458 | Missense Mutation | ACC,ATC | T,I 310 | NP_001243363.1 | |
NM_001256435.2 | 1458 | Missense Mutation | ACC,ATC | T,I 273 | NP_001243364.1 | |
NM_001282203.1 | 1458 | Missense Mutation | ACC,ATC | T,I 273 | NP_001269132.1 | |
NM_001282204.1 | 1458 | Missense Mutation | ACC,ATC | T,I 319 | NP_001269133.1 | |
NM_002861.4 | 1458 | Missense Mutation | ACC,ATC | T,I 351 | NP_002852.1 | |
XM_005256386.3 | 1458 | Missense Mutation | ACC,ATC | T,I 337 | XP_005256443.1 | |
XM_005256387.3 | 1458 | Missense Mutation | ACC,ATC | T,I 337 | XP_005256444.1 | |
XM_006722287.3 | 1458 | Missense Mutation | ACC,ATC | T,I 347 | XP_006722350.1 | |
XM_017024910.1 | 1458 | Missense Mutation | ACC,ATC | T,I 329 | XP_016880399.1 | |
XM_017024911.1 | 1458 | Missense Mutation | ACC,ATC | T,I 319 | XP_016880400.1 | |
XM_017024912.1 | 1458 | Missense Mutation | ACC,ATC | T,I 182 | XP_016880401.1 |
SIRT7 - sirtuin 7 | ||||||
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There are no transcripts associated with this gene. |