Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTATAATGGGTTTGTCCTGCCATG[C/T]TTGGGTGTTCATCCAGTTCAAGGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 609174 | ||||||||||||||||||||
Literature Links: |
NSL1 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 |
NSL1 - NSL1, MIS12 kinetochore complex component | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042549.1 | 287 | Intron | NP_001036014.1 | |||
NM_001297736.1 | 287 | Intron | NP_001284665.1 | |||
NM_001297737.1 | 287 | Intron | NP_001284666.1 | |||
NM_001297739.1 | 287 | Intron | NP_001284668.1 | |||
NM_015471.3 | 287 | Intron | NP_056286.3 | |||
XM_017000968.1 | 287 | Intron | XP_016856457.1 | |||
XM_017000969.1 | 287 | Intron | XP_016856458.1 |
TATDN3 - TatD DNase domain containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042552.2 | 287 | Silent Mutation | TGC,TGT | C,C 66 | NP_001036017.1 | |
NM_001042553.2 | 287 | Silent Mutation | TGC,TGT | C,C 66 | NP_001036018.1 | |
NM_001146169.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | NP_001139641.1 | |
NM_001146170.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | NP_001139642.1 | |
NM_001146171.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | NP_001139643.1 | |
XM_011509202.2 | 287 | Silent Mutation | TGC,TGT | C,C 66 | XP_011507504.1 | |
XM_017000328.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | XP_016855817.1 | |
XM_017000329.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | XP_016855818.1 | |
XM_017000330.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | XP_016855819.1 | |
XM_017000331.1 | 287 | Silent Mutation | TGC,TGT | C,C 66 | XP_016855820.1 |