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GCTCTGAAGTGGACTTTGAACTTGG[C/T]TCCTGCTGTTTTCAGAAACCATGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603817 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASAP2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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ASAP2 - ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135191.1 | Intron | NP_001128663.1 | ||||
NM_003887.2 | Intron | NP_003878.1 | ||||
XM_006711898.1 | Intron | XP_006711961.1 | ||||
XM_006711901.3 | Intron | XP_006711964.1 | ||||
XM_006711902.1 | Intron | XP_006711965.1 | ||||
XM_011510403.2 | Intron | XP_011508705.1 | ||||
XM_011510404.2 | Intron | XP_011508706.1 | ||||
XM_011510405.2 | Intron | XP_011508707.1 | ||||
XM_011510406.2 | Intron | XP_011508708.1 | ||||
XM_011510407.2 | Intron | XP_011508709.1 | ||||
XM_011510408.2 | Intron | XP_011508710.1 | ||||
XM_011510409.1 | Intron | XP_011508711.1 |