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TGTAGAAGCAGAATTCCAGCAGGTC[A/G]CTCACCAGCTGTAACACAGACACAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609746 MIM: 600983 | ||||||||||||||||||||
Literature Links: |
ARHGAP10 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 |
ARHGAP10 - Rho GTPase activating protein 10 | ||||||
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There are no transcripts associated with this gene. |
NR3C2 - nuclear receptor subfamily 3 group C member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000901.4 | 3468 | Silent Mutation | AGC,AGT | S,S 936 | NP_000892.2 | |
NM_001166104.1 | 3468 | Silent Mutation | AGC,AGT | S,S 819 | NP_001159576.1 | |
XM_011531975.1 | 3468 | Silent Mutation | AGC,AGT | S,S 940 | XP_011530277.1 | |
XM_011531976.2 | 3468 | Silent Mutation | AGC,AGT | S,S 940 | XP_011530278.1 | |
XM_011531977.2 | 3468 | Silent Mutation | AGC,AGT | S,S 940 | XP_011530279.1 | |
XM_011531978.2 | 3468 | Intron | XP_011530280.1 | |||
XM_017008217.1 | 3468 | Silent Mutation | AGC,AGT | S,S 936 | XP_016863706.1 |