Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCAAAGACAACATGGCCCAGGAGGG[C/T]GTGATTCTGGACGACGTGGACAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615051 MIM: 613560 | ||||||||||||||||||||
Literature Links: |
ASB6 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 |
ASB6 - ankyrin repeat and SOCS box containing 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001202403.1 | 742 | UTR 3 | NP_001189332.1 | |||
NM_017873.3 | 742 | UTR 3 | NP_060343.1 | |||
NM_177999.2 | 742 | UTR 3 | NP_821066.1 |
NTMT1 - N-terminal Xaa-Pro-Lys N-methyltransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286796.1 | 742 | Silent Mutation | GGC,GGT | G,G 173 | NP_001273725.1 | |
NM_001286797.1 | 742 | Silent Mutation | GGC,GGT | G,G 173 | NP_001273726.1 | |
NM_001286798.1 | 742 | Silent Mutation | GGC,GGT | G,G 173 | NP_001273727.1 | |
NM_001286799.1 | 742 | Silent Mutation | GGC,GGT | G,G 173 | NP_001273728.1 | |
NM_001286800.1 | 742 | Missense Mutation | GCG,GTG | A,V 145 | NP_001273729.1 | |
NM_001286801.1 | 742 | Missense Mutation | GCG,GTG | A,V 145 | NP_001273730.1 | |
NM_001286802.1 | 742 | Silent Mutation | GGC,GGT | G,G 85 | NP_001273731.1 | |
NM_001286803.1 | 742 | Silent Mutation | GGC,GGT | G,G 85 | NP_001273732.1 | |
NM_014064.3 | 742 | Silent Mutation | GGC,GGT | G,G 173 | NP_054783.2 | |
XM_005251939.3 | 742 | Silent Mutation | GGC,GGT | G,G 85 | XP_005251996.1 | |
XM_017014642.1 | 742 | Intron | XP_016870131.1 |