Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCACTGGGTCATCCTCATAGATAT[A/T]AAGCGGTTCACTTGGAGATAAGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612878 | ||||||||||||||||||||
Literature Links: |
EXPH5 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 |
EXPH5 - exophilin 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144763.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | NP_001138235.1 | |
NM_001144764.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1801 | NP_001138236.1 | |
NM_001144765.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1769 | NP_001138237.1 | |
NM_001308019.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1950 | NP_001294948.1 | |
NM_015065.2 | 5980 | Missense Mutation | AAT,TAT | N,Y 1957 | NP_055880.2 | |
XM_011542696.2 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_011540998.1 | |
XM_011542698.2 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_011541000.1 | |
XM_011542700.2 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_011541002.1 | |
XM_017017397.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_016872886.1 | |
XM_017017398.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1880 | XP_016872887.1 | |
XM_017017399.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_016872888.1 | |
XM_017017400.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1881 | XP_016872889.1 | |
XM_017017401.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1880 | XP_016872890.1 | |
XM_017017402.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1801 | XP_016872891.1 | |
XM_017017403.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1800 | XP_016872892.1 | |
XM_017017404.1 | 5980 | Missense Mutation | AAT,TAT | N,Y 1769 | XP_016872893.1 |