Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATGGTCACCAAGAAAAAGAATCTG[A/G]CCTTCTTGAGGTCTAGACTCTATAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGEF38 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
ARHGEF38 - Rho guanine nucleotide exchange factor 38 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242729.1 | 219 | Missense Mutation | ACC,GCC | T,A 20 | NP_001229658.1 | |
NM_017700.1 | 219 | Missense Mutation | ACC,GCC | T,A 20 | NP_060170.1 | |
XM_006714244.3 | 219 | Intron | XP_006714307.1 | |||
XM_011532050.2 | 219 | Intron | XP_011530352.1 | |||
XM_011532051.2 | 219 | Missense Mutation | ACC,GCC | T,A 20 | XP_011530353.1 |
ARHGEF38-IT1 - ARHGEF38 intronic transcript 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |