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ATCATTGTCTATATCCAGCAGGATG[C/T]GGCCAGGCACGTCTTTGCTGGCTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608293 MIM: 610238 | ||||||||||||||||||||
Literature Links: |
ARHGAP17 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 |
ARHGAP17 - Rho GTPase activating protein 17 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006634.2 | 2621 | Missense Mutation | CAC,CGC | H,R 867 | NP_001006635.1 | |
NM_018054.5 | 2621 | Missense Mutation | CAC,CGC | H,R 789 | NP_060524.4 | |
XM_011545873.2 | 2621 | Missense Mutation | CAC,CGC | H,R 899 | XP_011544175.1 | |
XM_011545874.2 | 2621 | Missense Mutation | CAC,CGC | H,R 898 | XP_011544176.1 | |
XM_011545875.2 | 2621 | UTR 3 | XP_011544177.1 | |||
XM_011545876.2 | 2621 | UTR 3 | XP_011544178.1 | |||
XM_011545877.2 | 2621 | Missense Mutation | CAC,CGC | H,R 822 | XP_011544179.1 | |
XM_011545878.2 | 2621 | Missense Mutation | CAC,CGC | H,R 821 | XP_011544180.1 | |
XM_017023390.1 | 2621 | UTR 3 | XP_016878879.1 |
SLC5A11 - solute carrier family 5 member 11 | ||||||
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There are no transcripts associated with this gene. |