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CAACTGAATGCAAAGGGGTTAAGTA[A/G]GTTGCCCAGCATCACATAATGAGTG
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | Intron | NP_071926.4 | ||||
XM_005268497.1 | Intron | XP_005268554.1 | ||||
XM_005268498.1 | Intron | XP_005268555.1 | ||||
XM_005268499.1 | Intron | XP_005268556.1 | ||||
XM_005268500.3 | Intron | XP_005268557.1 | ||||
XM_006714792.1 | Intron | XP_006714855.1 | ||||
XM_011537677.2 | Intron | XP_011535979.1 |
FCHSD1 - FCH and double SH3 domains 1 | ||||||
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There are no transcripts associated with this gene. |