Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGACACAGCTTCTAGTGTTGCTTTG[A/G]ATCTTGTGGAAAGTCAGAGTAAGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
NSMCE2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
NSMCE2 - NSE2/MMS21 homolog, SMC5-SMC6 complex SUMO ligase | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173685.2 | 405 | Missense Mutation | AAT,GAT | N,D 47 | NP_775956.1 | |
XM_005250875.2 | 405 | Missense Mutation | AAT,GAT | N,D 47 | XP_005250932.1 | |
XM_005250876.4 | 405 | Missense Mutation | AAT,GAT | N,D 47 | XP_005250933.1 | |
XM_011516974.2 | 405 | Missense Mutation | AAT,GAT | N,D 47 | XP_011515276.1 | |
XM_011516975.1 | 405 | Missense Mutation | AAT,GAT | N,D 47 | XP_011515277.1 | |
XM_017013330.1 | 405 | Intron | XP_016868819.1 | |||
XM_017013331.1 | 405 | Missense Mutation | AAT,GAT | N,D 47 | XP_016868820.1 | |
XM_017013332.1 | 405 | Intron | XP_016868821.1 | |||
XM_017013333.1 | 405 | UTR 5 | XP_016868822.1 | |||
XM_017013334.1 | 405 | Intron | XP_016868823.1 |