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CGTTCCTTCTGGGCAGAGGCTGCCT[A/G]GCTGAGGGACCATCTTCAGGGCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 616594 MIM: 604128 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASAP3 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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ASAP3 - ArfGAP with SH3 domain, ankyrin repeat and PH domain 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143778.1 | 2731 | Silent Mutation | GCC,GCT | A,A 860 | NP_001137250.1 | |
NM_017707.3 | 2731 | Silent Mutation | GCC,GCT | A,A 869 | NP_060177.2 | |
XM_011541755.1 | 2731 | Silent Mutation | GCC,GCT | A,A 892 | XP_011540057.1 | |
XM_017001685.1 | 2731 | Silent Mutation | GCC,GCT | A,A 890 | XP_016857174.1 | |
XM_017001686.1 | 2731 | Silent Mutation | GCC,GCT | A,A 871 | XP_016857175.1 | |
XM_017001687.1 | 2731 | Silent Mutation | GCC,GCT | A,A 849 | XP_016857176.1 | |
XM_017001688.1 | 2731 | Silent Mutation | GCC,GCT | A,A 759 | XP_016857177.1 | |
XM_017001689.1 | 2731 | Silent Mutation | GCC,GCT | A,A 740 | XP_016857178.1 |
TCEA3 - transcription elongation factor A3 | ||||||
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There are no transcripts associated with this gene. |