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ATGGCGGCCGGCAAGAGCGGCGGTA[G/T]CGCAGGGGAGATTACTTTTCTGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605003 | ||||||||||||||||||||
Literature Links: |
SENP6 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 |
SENP6 - SUMO1/sentrin specific peptidase 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100409.2 | 687 | Missense Mutation | AGC,ATC | S,I 9 | NP_001093879.1 | |
NM_001304792.1 | 687 | Missense Mutation | AGC,ATC | S,I 9 | NP_001291721.1 | |
NM_015571.3 | 687 | Missense Mutation | AGC,ATC | S,I 9 | NP_056386.2 | |
XM_006715457.3 | 687 | UTR 5 | XP_006715520.1 | |||
XM_011535746.2 | 687 | Missense Mutation | AGC,ATC | S,I 9 | XP_011534048.1 | |
XM_011535747.2 | 687 | UTR 5 | XP_011534049.1 | |||
XM_017010719.1 | 687 | Missense Mutation | AGC,ATC | S,I 9 | XP_016866208.1 | |
XM_017010720.1 | 687 | Intron | XP_016866209.1 | |||
XM_017010721.1 | 687 | Intron | XP_016866210.1 | |||
XM_017010722.1 | 687 | UTR 5 | XP_016866211.1 | |||
XM_017010723.1 | 687 | UTR 5 | XP_016866212.1 | |||
XM_017010724.1 | 687 | UTR 5 | XP_016866213.1 | |||
XM_017010725.1 | 687 | UTR 5 | XP_016866214.1 |