Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCAGAGTTGCTCAGCCTTGAGTGC[A/C]CAACCGTGAGAATGGAGCGTGCCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605370 | ||||||||||||||||||||
Literature Links: |
ARHGAP26 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 |
ARHGAP26 - Rho GTPase activating protein 26 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135608.1 | 372 | Intron | NP_001129080.1 | |||
NM_015071.4 | 372 | Intron | NP_055886.1 | |||
XM_005268398.4 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_005268455.1 | |
XM_005268399.4 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_005268456.1 | |
XM_005268400.4 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_005268457.1 | |
XM_005268402.4 | 372 | Intron | XP_005268459.1 | |||
XM_006714774.3 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_006714837.1 | |
XM_011537610.2 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_011535912.1 | |
XM_011537611.2 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_011535913.1 | |
XM_011537612.2 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_011535914.1 | |
XM_017009247.1 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_016864736.1 | |
XM_017009248.1 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_016864737.1 | |
XM_017009249.1 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_016864738.1 | |
XM_017009250.1 | 372 | Missense Mutation | ACA,CCA | T,P 76 | XP_016864739.1 |