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GTCCACCGCTCCGGGATGTGGGTCT[A/G]CTGGAGGCGGGCAGTGTGCCCGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
8 submissions
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Phenotype: |
MIM: 604266 | ||||||||||||||||||||
Literature Links: |
ARHGEF16 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 |
ARHGEF16 - Rho guanine nucleotide exchange factor 16 | ||||||
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There are no transcripts associated with this gene. |
MEGF6 - multiple EGF like domains 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001409.3 | 4449 | Silent Mutation | AGC,AGT | S,S 1529 | NP_001400.3 | |
XM_006710406.3 | 4449 | Silent Mutation | AGC,AGT | S,S 1424 | XP_006710469.1 | |
XM_011540885.1 | 4449 | Silent Mutation | AGC,AGT | S,S 1591 | XP_011539187.1 | |
XM_011540886.1 | 4449 | Silent Mutation | AGC,AGT | S,S 1548 | XP_011539188.1 | |
XM_011540887.2 | 4449 | Silent Mutation | AGC,AGT | S,S 1383 | XP_011539189.1 | |
XM_011540888.2 | 4449 | Intron | XP_011539190.1 | |||
XM_017000533.1 | 4449 | Silent Mutation | AGC,AGT | S,S 1547 | XP_016856022.1 |