Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCAACAAGCTGTCTCACGGCATT[C/G]ATTTCAGTTGGACTCAGCTGGGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603577 | ||||||||||||||||||||
Literature Links: |
NOL4 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 |
NOL4 - nucleolar protein 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198546.1 | 1856 | Silent Mutation | ATC,ATG | I,M 542 | NP_001185475.1 | |
NM_001198547.1 | 1856 | Silent Mutation | ATC,ATG | I,M 532 | NP_001185476.1 | |
NM_001198548.1 | 1856 | Silent Mutation | ATC,ATG | I,M 504 | NP_001185477.1 | |
NM_001198549.1 | 1856 | Silent Mutation | ATC,ATG | I,M 321 | NP_001185478.1 | |
NM_001282527.1 | 1856 | Silent Mutation | ATC,ATG | I,M 387 | NP_001269456.1 | |
NM_003787.4 | 1856 | Silent Mutation | ATC,ATG | I,M 606 | NP_003778.2 | |
XM_006722563.2 | 1856 | Silent Mutation | ATC,ATG | I,M 606 | XP_006722626.1 | |
XM_006722564.2 | 1856 | Silent Mutation | ATC,ATG | I,M 468 | XP_006722627.1 | |
XM_006722565.1 | 1856 | Silent Mutation | ATC,ATG | I,M 451 | XP_006722628.1 | |
XM_011526237.1 | 1856 | Missense Mutation | ATC,ATG | I,M 606 | XP_011524539.1 | |
XM_011526238.1 | 1856 | Silent Mutation | ATC,ATG | I,M 492 | XP_011524540.1 | |
XM_011526239.2 | 1856 | Silent Mutation | ATC,ATG | I,M 451 | XP_011524541.1 | |
XM_017026052.1 | 1856 | Silent Mutation | ATC,ATG | I,M 486 | XP_016881541.1 | |
XM_017026053.1 | 1856 | Silent Mutation | ATC,ATG | I,M 451 | XP_016881542.1 | |
XM_017026054.1 | 1856 | Silent Mutation | ATC,ATG | I,M 451 | XP_016881543.1 | |
XM_017026055.1 | 1856 | Silent Mutation | ATC,ATG | I,M 387 | XP_016881544.1 | |
XM_017026056.1 | 1856 | Silent Mutation | ATC,ATG | I,M 387 | XP_016881545.1 | |
XM_017026057.1 | 1856 | Silent Mutation | ATC,ATG | I,M 355 | XP_016881546.1 | |
XM_017026058.1 | 1856 | Silent Mutation | ATC,ATG | I,M 451 | XP_016881547.1 | |
XM_017026059.1 | 1856 | Silent Mutation | ATC,ATG | I,M 321 | XP_016881548.1 | |
XM_017026060.1 | 1856 | Silent Mutation | ATC,ATG | I,M 291 | XP_016881549.1 |