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Search Thermo Fisher Scientific
GTTCTGGGGATGGGCCAGGACATCA[A/C]ACAGAGCCTTGATAAGTTTCTTATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611747 | ||||||||||||||||||||
Literature Links: |
SCUBE2 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 |
SCUBE2 - signal peptide, CUB domain and EGF like domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170690.1 | 3031 | Missense Mutation | TGT,TTT | C,F 766 | NP_001164161.1 | |
NM_020974.2 | 3031 | Missense Mutation | TGT,TTT | C,F 930 | NP_066025.2 | |
XM_005253032.4 | 3031 | Missense Mutation | TGT,TTT | C,F 987 | XP_005253089.2 | |
XM_005253033.4 | 3031 | Missense Mutation | TGT,TTT | C,F 958 | XP_005253090.2 | |
XM_005253034.4 | 3031 | Missense Mutation | TGT,TTT | C,F 946 | XP_005253091.2 | |
XM_005253035.4 | 3031 | Intron | XP_005253092.2 | |||
XM_005253036.4 | 3031 | Missense Mutation | TGT,TTT | C,F 878 | XP_005253093.2 | |
XM_005253037.4 | 3031 | Missense Mutation | TGT,TTT | C,F 832 | XP_005253094.2 | |
XM_011520246.2 | 3031 | Missense Mutation | TGT,TTT | C,F 921 | XP_011518548.1 | |
XM_011520247.2 | 3031 | Missense Mutation | TGT,TTT | C,F 919 | XP_011518549.1 | |
XM_011520248.2 | 3031 | Intron | XP_011518550.1 | |||
XM_017018080.1 | 3031 | Missense Mutation | TGT,TTT | C,F 917 | XP_016873569.1 | |
XM_017018081.1 | 3031 | Missense Mutation | TGT,TTT | C,F 851 | XP_016873570.1 | |
XM_017018082.1 | 3031 | Intron | XP_016873571.1 |