Search Thermo Fisher Scientific
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TCCACAATGAGCTGCGGGGCGACGT[C/T]ATTCCCCGAGGGTCTAACTTGCGCT
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 - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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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 | 251 | Silent Mutation | GTC,GTT | V,V 68 | NP_001257325.1 | |
NM_152436.2 | 251 | Silent Mutation | GTC,GTT | V,V 68 | NP_689649.1 | |
XM_011537949.2 | 251 | Intron | XP_011536251.1 | |||
XM_011537950.2 | 251 | Intron | XP_011536252.1 | |||
XM_017018848.1 | 251 | UTR 5 | XP_016874337.1 | |||
XM_017018849.1 | 251 | Intron | XP_016874338.1 |
Set Membership: |
HapMap |