Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCACCAGGAAAGCAGTCAGGAAA[C/T]GAAGCACCTGGTAGTTCTCCTCGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 602732 MIM: 615088 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARHGAP1 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
|
ARHGAP1 - Rho GTPase activating protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004308.3 | 1023 | Missense Mutation | CAT,CGT | H,R 369 | NP_004299.1 | |
XM_011520095.1 | 1023 | Missense Mutation | CAT,CGT | H,R 369 | XP_011518397.1 | |
XM_017017720.1 | 1023 | Missense Mutation | CAT,CGT | H,R 325 | XP_016873209.1 |
ATG13 - autophagy related 13 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |