Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147559 MIM: 180190 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ITGB7 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 | 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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ITGB7 - integrin subunit beta 7 | ||||||
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There are no transcripts associated with this gene. |
RARG - retinoic acid receptor gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000966.5 | 1446 | Missense Mutation | TCG,TTG | S,L 427 | NP_000957.1 | |
NM_001042728.2 | 1446 | Missense Mutation | TCG,TTG | S,L 416 | NP_001036193.1 | |
NM_001243730.1 | 1446 | Missense Mutation | TCG,TTG | S,L 355 | NP_001230659.1 | |
NM_001243731.1 | 1446 | Missense Mutation | TCG,TTG | S,L 306 | NP_001230660.1 | |
NM_001243732.1 | 1446 | Missense Mutation | TCG,TTG | S,L 405 | NP_001230661.1 |
Set Membership: |
HapMap |