Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGAGGCATCGGGCCTGGAATCTCC[A/G]TCTTCAGAGTAATGGCCCTTTCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 147559 MIM: 180190 | ||||||||||||||||||||
Literature Links: |
ITGB7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
ITGB7 - integrin subunit beta 7 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
RARG - retinoic acid receptor gamma | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000966.5 | 1371 | Missense Mutation | ACG,ATG | T,M 402 | NP_000957.1 | |
NM_001042728.2 | 1371 | Missense Mutation | ACG,ATG | T,M 391 | NP_001036193.1 | |
NM_001243730.1 | 1371 | Missense Mutation | ACG,ATG | T,M 330 | NP_001230659.1 | |
NM_001243731.1 | 1371 | Missense Mutation | ACG,ATG | T,M 281 | NP_001230660.1 | |
NM_001243732.1 | 1371 | Missense Mutation | ACG,ATG | T,M 380 | NP_001230661.1 |