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ATGAGATGAACCATCTTCCTGCACA[C/T]AGCCAAAGTCTGCAAAGGTGATGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SP140L PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SP140L - SP140 nuclear body protein like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308162.1 | 167 | Intron | NP_001295091.1 | |||
NM_001308163.1 | 167 | Intron | NP_001295092.1 | |||
NM_138402.4 | 167 | Silent Mutation | CAC,CAT | H,H 30 | NP_612411.4 | |
XM_006712855.2 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_006712918.1 | |
XM_006712856.2 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_006712919.1 | |
XM_006712858.3 | 167 | Intron | XP_006712921.1 | |||
XM_011512190.2 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_011510492.1 | |
XM_011512191.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_011510493.1 | |
XM_017005294.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860783.1 | |
XM_017005295.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860784.1 | |
XM_017005296.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860785.1 | |
XM_017005297.1 | 167 | Intron | XP_016860786.1 | |||
XM_017005298.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860787.1 | |
XM_017005299.1 | 167 | Intron | XP_016860788.1 | |||
XM_017005300.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860789.1 | |
XM_017005301.1 | 167 | Silent Mutation | CAC,CAT | H,H 30 | XP_016860790.1 |