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Search Thermo Fisher Scientific
TCTTCAGGGCTCCGCGCCCCCCGCC[A/G]ATAGGAGCGAGTGCTCTCGGAGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
9 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 |
---|---|---|
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 |
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 | 2693 | Missense Mutation | CGG,TGG | R,W 848 | NP_001137250.1 | |
NM_017707.3 | 2693 | Missense Mutation | CGG,TGG | R,W 857 | NP_060177.2 | |
XM_011541755.1 | 2693 | Missense Mutation | CGG,TGG | R,W 880 | XP_011540057.1 | |
XM_017001685.1 | 2693 | Missense Mutation | CGG,TGG | R,W 878 | XP_016857174.1 | |
XM_017001686.1 | 2693 | Missense Mutation | CGG,TGG | R,W 859 | XP_016857175.1 | |
XM_017001687.1 | 2693 | Missense Mutation | CGG,TGG | R,W 837 | XP_016857176.1 | |
XM_017001688.1 | 2693 | Missense Mutation | CGG,TGG | R,W 747 | XP_016857177.1 | |
XM_017001689.1 | 2693 | Missense Mutation | CGG,TGG | R,W 728 | XP_016857178.1 |
TCEA3 - transcription elongation factor A3 | ||||||
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There are no transcripts associated with this gene. |