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GGACAGGGTCCTCCGGTTGTGTAGT[C/T]GCCGCTGGACACAGGTGGGGTGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606647 | ||||||||||||||||||||
Literature Links: |
ARAP3 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 |
ARAP3 - ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022481.5 | 3612 | Missense Mutation | CAA,CGA | Q,R 1372 | NP_071926.4 | |
XM_005268497.1 | 3612 | Intron | XP_005268554.1 | |||
XM_005268498.1 | 3612 | Missense Mutation | CAA,CGA | Q,R 1352 | XP_005268555.1 | |
XM_005268499.1 | 3612 | Missense Mutation | CAA,CGA | Q,R 1294 | XP_005268556.1 | |
XM_005268500.3 | 3612 | Intron | XP_005268557.1 | |||
XM_006714792.1 | 3612 | Missense Mutation | CAA,CGA | Q,R 1301 | XP_006714855.1 | |
XM_011537677.2 | 3612 | Missense Mutation | CAA,CGA | Q,R 1177 | XP_011535979.1 |
FCHSD1 - FCH and double SH3 domains 1 | ||||||
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There are no transcripts associated with this gene. |