Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGATGCACCAACCCCAATGTGCACC[C/G]CCATCTTCTGGGAGCCCCCAGCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608504 | ||||||||||||||||||||
Literature Links: |
ARHGEF15 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 |
ARHGEF15 - Rho guanine nucleotide exchange factor 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025014.1 | 269 | Missense Mutation | CCC,GCC | P,A 60 | NP_079290.1 | |
NM_173728.3 | 269 | Missense Mutation | CCC,GCC | P,A 60 | NP_776089.2 | |
XM_011523734.1 | 269 | Missense Mutation | CCC,GCC | P,A 60 | XP_011522036.1 | |
XM_011523735.1 | 269 | Missense Mutation | CCC,GCC | P,A 60 | XP_011522037.1 | |
XM_011523736.1 | 269 | Missense Mutation | CCC,GCC | P,A 60 | XP_011522038.1 | |
XM_011523737.1 | 269 | Intron | XP_011522039.1 |