Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGGGAAAGCAGCACCTACTTGGAGT[C/T]GGGGGCCAGGTGGTCCAGGCAGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
IQGAP3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
IQGAP3 - IQ motif containing GTPase activating protein 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178229.4 | 4628 | Missense Mutation | AAC,GAC | N,D 1522 | NP_839943.2 | |
XM_011509198.2 | 4628 | Missense Mutation | AAC,GAC | N,D 1527 | XP_011507500.1 | |
XM_011509200.2 | 4628 | Missense Mutation | AAC,GAC | N,D 1080 | XP_011507502.1 | |
XM_011509201.2 | 4628 | Missense Mutation | AAC,GAC | N,D 1026 | XP_011507503.1 | |
XM_017000317.1 | 4628 | Missense Mutation | AAC,GAC | N,D 1526 | XP_016855806.1 | |
XM_017000318.1 | 4628 | Missense Mutation | AAC,GAC | N,D 1388 | XP_016855807.1 |