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ACTGACTATCCCAGTGTCTGTGCCC[A/G]CCGTCCAAGCTGACAGCTGCTCTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603817 MIM: 607153 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASAP2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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ASAP2 - ArfGAP with SH3 domain, ankyrin repeat and PH domain 2 | ||||||
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There are no transcripts associated with this gene. |
ITGB1BP1 - integrin subunit beta 1 binding protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319066.1 | Intron | NP_001305995.1 | ||||
NM_001319067.1 | Intron | NP_001305996.1 | ||||
NM_001319068.1 | Intron | NP_001305997.1 | ||||
NM_001319069.1 | Intron | NP_001305998.1 | ||||
NM_001319070.1 | Intron | NP_001305999.1 | ||||
NM_004763.4 | Intron | NP_004754.1 | ||||
NM_022334.4 | Intron | NP_071729.1 | ||||
XM_005246183.4 | Intron | XP_005246240.1 | ||||
XM_005246184.4 | Intron | XP_005246241.1 | ||||
XM_005246185.4 | Intron | XP_005246242.1 | ||||
XM_005246189.4 | Intron | XP_005246246.1 | ||||
XM_006711903.3 | Intron | XP_006711966.1 | ||||
XM_011510416.2 | Intron | XP_011508718.1 | ||||
XM_017005267.1 | Intron | XP_016860756.1 | ||||
XM_017005268.1 | Intron | XP_016860757.1 | ||||
XM_017005269.1 | Intron | XP_016860758.1 | ||||
XM_017005270.1 | Intron | XP_016860759.1 |