Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTGGGGGCAGCGACCTGAGCACC[A/G]GGTGAGTCTTTATCTCTCTTCCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
SP140L 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 |
SP140L - SP140 nuclear body protein like | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308162.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | NP_001295091.1 | |
NM_001308163.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | NP_001295092.1 | |
NM_138402.4 | 108 | Missense Mutation | AGG,GGG | R,G 11 | NP_612411.4 | |
XM_006712855.2 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_006712918.1 | |
XM_006712856.2 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_006712919.1 | |
XM_006712858.3 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_006712921.1 | |
XM_011512190.2 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_011510492.1 | |
XM_011512191.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_011510493.1 | |
XM_017005294.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860783.1 | |
XM_017005295.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860784.1 | |
XM_017005296.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860785.1 | |
XM_017005297.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860786.1 | |
XM_017005298.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860787.1 | |
XM_017005299.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860788.1 | |
XM_017005300.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860789.1 | |
XM_017005301.1 | 108 | Missense Mutation | AGG,GGG | R,G 11 | XP_016860790.1 |