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GCGCTCAACCACCTAAAAGCCAGCA[A/C]ATCTGTTAGCAAACTTCCAAAGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604980 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RACGAP1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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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
|
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AMR
|
RACGAP1 - Rac GTPase activating protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001126103.2 | Intron | NP_001119575.1 | ||||
NM_001126104.2 | Intron | NP_001119576.1 | ||||
NM_001319999.1 | Intron | NP_001306928.1 | ||||
NM_001320000.1 | Intron | NP_001306929.1 | ||||
NM_001320001.1 | Intron | NP_001306930.1 | ||||
NM_001320002.1 | Intron | NP_001306931.1 | ||||
NM_001320003.1 | Intron | NP_001306932.1 | ||||
NM_001320004.1 | Intron | NP_001306933.1 | ||||
NM_001320005.1 | Intron | NP_001306934.1 | ||||
NM_001320006.1 | Intron | NP_001306935.1 | ||||
NM_001320007.1 | Intron | NP_001306936.1 | ||||
NM_013277.4 | Intron | NP_037409.2 | ||||
XM_006719359.1 | Intron | XP_006719422.1 | ||||
XM_011538238.1 | Intron | XP_011536540.1 | ||||
XM_011538243.1 | Intron | XP_011536545.1 | ||||
XM_017019220.1 | Intron | XP_016874709.1 | ||||
XM_017019221.1 | Intron | XP_016874710.1 | ||||
XM_017019222.1 | Intron | XP_016874711.1 | ||||
XM_017019223.1 | Intron | XP_016874712.1 | ||||
XM_017019224.1 | Intron | XP_016874713.1 | ||||
XM_017019225.1 | Intron | XP_016874714.1 | ||||
XM_017019226.1 | Intron | XP_016874715.1 | ||||
XM_017019227.1 | Intron | XP_016874716.1 |