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AGCAGATGAAACAAAGGACTATATG[A/C]ATCAACTTTCACATGAAGTACTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608533 | ||||||||||||||||||||
Literature Links: |
FBXO38 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 |
FBXO38 - F-box protein 38 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271723.1 | 237 | Missense Mutation | AAT,CAT | N,H 31 | NP_001258652.1 | |
NM_030793.4 | 237 | Missense Mutation | AAT,CAT | N,H 31 | NP_110420.3 | |
XM_005268513.1 | 237 | Missense Mutation | AAT,CAT | N,H 31 | XP_005268570.1 | |
XM_006714797.1 | 237 | Missense Mutation | AAT,CAT | N,H 31 | XP_006714860.1 | |
XM_011537684.2 | 237 | Intron | XP_011535986.1 | |||
XM_017009899.1 | 237 | UTR 5 | XP_016865388.1 | |||
XM_017009900.1 | 237 | Intron | XP_016865389.1 | |||
XM_017009901.1 | 237 | Intron | XP_016865390.1 | |||
XM_017009902.1 | 237 | Intron | XP_016865391.1 |