Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCCATCCCCACAGGCGACAGCTG[G/T]CCAAGCTGGCCATCATCTTCAGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608453 | ||||||||||||||||||||
Literature Links: |
CBLC 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 |
CBLC - Cbl proto-oncogene C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130852.1 | 441 | Missense Mutation | GCC,TCC | A,S 122 | NP_001124324.1 | |
NM_012116.3 | 441 | Missense Mutation | GCC,TCC | A,S 122 | NP_036248.3 | |
XM_005258696.3 | 441 | Missense Mutation | GCC,TCC | A,S 122 | XP_005258753.1 | |
XM_011526688.2 | 441 | Missense Mutation | GCC,TCC | A,S 122 | XP_011524990.1 | |
XM_011526689.2 | 441 | Missense Mutation | GCC,TCC | A,S 122 | XP_011524991.1 | |
XM_011526690.2 | 441 | Missense Mutation | GCC,TCC | A,S 122 | XP_011524992.1 |