Search Thermo Fisher Scientific
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GGAGGCAGACCCCCGCGGCGCCGTG[A/C]GTGAATCTGCTCGCTGATCTGCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
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Literature Links: |
SH3BP5L 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 |
SH3BP5L - SH3 binding domain protein 5 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322462.1 | 1257 | Missense Mutation | NP_001309391.1 | |||
NM_001322463.1 | 1257 | Missense Mutation | NP_001309392.1 | |||
NM_001322464.1 | 1257 | Missense Mutation | NP_001309393.1 | |||
NM_030645.1 | 1257 | Missense Mutation | NP_085148.1 | |||
XM_017002404.1 | 1257 | Missense Mutation | XP_016857893.1 | |||
XM_017002405.1 | 1257 | Missense Mutation | XP_016857894.1 | |||
XM_017002406.1 | 1257 | Missense Mutation | XP_016857895.1 | |||
XM_017002407.1 | 1257 | Missense Mutation | XP_016857896.1 |