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GGCTTCACTCACCATCCTCAGGGCA[A/G]GGCCCCAGTTCATGGCTGTTCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 605708 | ||||||||||||||||||||
Literature Links: |
ARHGEF11 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 |
ARHGEF11 - Rho guanine nucleotide exchange factor 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014784.3 | 4125 | Silent Mutation | CCC,CCT | P,P 1499 | NP_055599.1 | |
NM_198236.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1539 | NP_937879.1 | |
XM_005245629.4 | 4125 | Silent Mutation | CCC,CCT | P,P 1540 | XP_005245686.1 | |
XM_005245633.4 | 4125 | Silent Mutation | CCC,CCT | P,P 1118 | XP_005245690.1 | |
XM_006711659.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1556 | XP_006711722.1 | |
XM_006711660.3 | 4125 | Silent Mutation | CCC,CCT | P,P 1555 | XP_006711723.1 | |
XM_006711661.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1546 | XP_006711724.1 | |
XM_006711662.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1545 | XP_006711725.1 | |
XM_006711663.3 | 4125 | Silent Mutation | CCC,CCT | P,P 1536 | XP_006711726.1 | |
XM_006711665.3 | 4125 | Silent Mutation | CCC,CCT | P,P 1515 | XP_006711728.1 | |
XM_011510185.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1551 | XP_011508487.1 | |
XM_011510186.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1516 | XP_011508488.1 | |
XM_011510187.2 | 4125 | Silent Mutation | CCC,CCT | P,P 1462 | XP_011508489.1 | |
XM_011510189.2 | 4125 | Silent Mutation | CCC,CCT | P,P 922 | XP_011508491.1 | |
XM_017002920.1 | 4125 | Silent Mutation | CCC,CCT | P,P 1545 | XP_016858409.1 | |
XM_017002921.1 | 4125 | Silent Mutation | CCC,CCT | P,P 1529 | XP_016858410.1 | |
XM_017002922.1 | 4125 | Silent Mutation | CCC,CCT | P,P 1505 | XP_016858411.1 | |
XM_017002923.1 | 4125 | Silent Mutation | CCC,CCT | P,P 1500 | XP_016858412.1 | |
XM_017002924.1 | 4125 | Silent Mutation | CCC,CCT | P,P 1500 | XP_016858413.1 |
LRRC71 - leucine rich repeat containing 71 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144702.2 | 4125 | Intron | NP_653303.2 | |||
XM_005244926.3 | 4125 | Intron | XP_005244983.1 | |||
XM_005244927.3 | 4125 | Intron | XP_005244984.1 | |||
XM_005244928.2 | 4125 | Intron | XP_005244985.1 | |||
XM_006711185.3 | 4125 | Intron | XP_006711248.1 | |||
XM_006711186.3 | 4125 | Intron | XP_006711249.1 | |||
XM_006711187.3 | 4125 | Intron | XP_006711250.1 | |||
XM_011509239.2 | 4125 | Intron | XP_011507541.1 | |||
XM_011509240.2 | 4125 | Intron | XP_011507542.1 | |||
XM_011509241.2 | 4125 | Intron | XP_011507543.1 | |||
XM_017000459.1 | 4125 | Intron | XP_016855948.1 | |||
XM_017000460.1 | 4125 | Intron | XP_016855949.1 | |||
XM_017000461.1 | 4125 | Intron | XP_016855950.1 | |||
XM_017000462.1 | 4125 | Intron | XP_016855951.1 |
MIR765 - microRNA 765 | ||||||
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There are no transcripts associated with this gene. |