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CCCAAGGAAGGTCCTGCAGGAGGTC[C/T]GGAGAGTACTGAGACCGGTAAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600536 | ||||||||||||||||||||
Literature Links: |
ITGA7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ITGA7 - integrin subunit alpha 7 | ||||||
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There are no transcripts associated with this gene. |
METTL7B - methyltransferase like 7B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152637.2 | 690 | Missense Mutation | CGG,TGG | R,W 161 | NP_689850.2 |