Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATTTTCCAATGCCGCCTCAGGCCC[A/T]TGGGGTTTTCTGTGGTGAATTTCTG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604491 | |||||||||||||||||||||||
Literature Links: |
CBLB PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
CBLB - Cbl proto-oncogene B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321786.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 951 | NP_001308715.1 | |
NM_001321788.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 923 | NP_001308717.1 | |
NM_001321789.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 902 | NP_001308718.1 | |
NM_001321790.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 901 | NP_001308719.1 | |
NM_001321791.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 879 | NP_001308720.1 | |
NM_001321793.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 879 | NP_001308722.1 | |
NM_001321794.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 874 | NP_001308723.1 | |
NM_001321795.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 874 | NP_001308724.1 | |
NM_001321796.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 874 | NP_001308725.1 | |
NM_001321797.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 830 | NP_001308726.1 | |
NM_001321798.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 830 | NP_001308727.1 | |
NM_001321799.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 830 | NP_001308728.1 | |
NM_001321806.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 663 | NP_001308735.1 | |
NM_001321807.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 663 | NP_001308736.1 | |
NM_001321808.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 619 | NP_001308737.1 | |
NM_001321811.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 614 | NP_001308740.1 | |
NM_001321813.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 614 | NP_001308742.1 | |
NM_001321816.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 570 | NP_001308745.1 | |
NM_001321820.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 483 | NP_001308749.1 | |
NM_001321822.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 480 | NP_001308751.1 | |
NM_170662.4 | 2655 | Missense Mutation | CAA,CAT | Q,H 923 | NP_733762.2 | |
XM_011513257.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 923 | XP_011511559.1 | |
XM_011513259.2 | 2655 | Intron | XP_011511561.2 | |||
XM_017007395.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 945 | XP_016862884.1 | |
XM_017007396.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 907 | XP_016862885.1 | |
XM_017007397.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 902 | XP_016862886.1 | |
XM_017007398.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 896 | XP_016862887.1 | |
XM_017007399.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 874 | XP_016862888.1 | |
XM_017007400.1 | 2655 | Missense Mutation | CAA,CAT | Q,H 858 | XP_016862889.1 |