Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCGGTGGTACCCGTCTGTTTTCTT[G/T]TGCAAACTGTGATACGATCCTGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609726 | ||||||||||||||||||||
Literature Links: |
YPEL5 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 |
YPEL5 - yippee like 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127399.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | NP_001120871.1 | |
NM_001127400.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | NP_001120872.1 | |
NM_001127401.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | NP_001120873.1 | |
NM_016061.2 | 849 | Missense Mutation | TGT,TTT | C,F 17 | NP_057145.1 | |
XM_017004318.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | XP_016859807.1 | |
XM_017004319.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | XP_016859808.1 | |
XM_017004320.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | XP_016859809.1 | |
XM_017004321.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | XP_016859810.1 | |
XM_017004322.1 | 849 | Missense Mutation | TGT,TTT | C,F 17 | XP_016859811.1 |