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CTTAGCTTCGTCCTCTTTGTTGCTT[C/G]AACTTTCTTACATTCTTGGATGCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607724 MIM: 610394 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAPS2 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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YRI (Yoruba) - Not Available | ||||||
SAS
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Japanese
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CHB (Han Chinese) - Not Available | ||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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CAPS2 - calcyphosine 2 | ||||||
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There are no transcripts associated with this gene. |
GLIPR1L2 - GLI pathogenesis-related 1 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270396.1 | Intron | NP_001257325.1 | ||||
NM_152436.2 | Intron | NP_689649.1 | ||||
XM_011537949.2 | Intron | XP_011536251.1 | ||||
XM_011537950.2 | Intron | XP_011536252.1 | ||||
XM_017018848.1 | Intron | XP_016874337.1 | ||||
XM_017018849.1 | Intron | XP_016874338.1 |
Set Membership: |
Validated |