Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGTCGCTCTCCAGGCCCACGGGGC[C/T]CAGGGCGGGCGCGGCTGCCGCGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610591 | ||||||||||||||||||||
Literature Links: |
ARHGAP27 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 |
ARHGAP27 - Rho GTPase activating protein 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282290.1 | 2366 | Missense Mutation | AGC,GGC | S,G 656 | NP_001269219.1 | |
NM_174919.3 | 2366 | Intron | NP_777579.2 | |||
NM_199282.2 | 2366 | Missense Mutation | AGC,GGC | S,G 315 | NP_954976.1 | |
XM_005257128.3 | 2366 | Missense Mutation | AGC,GGC | S,G 434 | XP_005257185.1 | |
XM_006721745.2 | 2366 | Missense Mutation | AGC,GGC | S,G 656 | XP_006721808.1 | |
XM_006721747.2 | 2366 | Missense Mutation | AGC,GGC | S,G 634 | XP_006721810.1 | |
XM_006721750.3 | 2366 | Intron | XP_006721813.1 | |||
XM_011524468.1 | 2366 | Missense Mutation | AGC,GGC | S,G 689 | XP_011522770.1 | |
XM_011524469.1 | 2366 | Missense Mutation | AGC,GGC | S,G 667 | XP_011522771.1 | |
XM_011524470.2 | 2366 | Missense Mutation | AGC,GGC | S,G 689 | XP_011522772.1 | |
XM_011524471.1 | 2366 | Missense Mutation | AGC,GGC | S,G 632 | XP_011522773.1 | |
XM_011524472.2 | 2366 | Missense Mutation | AGC,GGC | S,G 489 | XP_011522774.1 | |
XM_011524473.2 | 2366 | Intron | XP_011522775.1 | |||
XM_011524474.1 | 2366 | Missense Mutation | AGC,GGC | S,G 348 | XP_011522776.1 | |
XM_017024311.1 | 2366 | Missense Mutation | AGC,GGC | S,G 689 | XP_016879800.1 | |
XM_017024312.1 | 2366 | Missense Mutation | AGC,GGC | S,G 456 | XP_016879801.1 | |
XM_017024313.1 | 2366 | Intron | XP_016879802.1 |