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GGGTTAACGGAAGCTTGGCCGCTCC[A/C]CATTGAGGAGGGCATGCTGGTGACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608486 MIM: 601445 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MTSS1 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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MTSS1 - metastasis suppressor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282971.1 | 2095 | Missense Mutation | GGG,TGG | G,W 669 | NP_001269900.1 | |
NM_001282974.1 | 2095 | Missense Mutation | GGG,TGG | G,W 640 | NP_001269903.1 | |
NM_014751.5 | 2095 | Missense Mutation | GGG,TGG | G,W 665 | NP_055566.3 | |
XM_005251111.1 | 2095 | Missense Mutation | GGG,TGG | G,W 778 | XP_005251168.1 | |
XM_005251113.1 | 2095 | Missense Mutation | GGG,TGG | G,W 713 | XP_005251170.1 | |
XM_005251118.1 | 2095 | Missense Mutation | GGG,TGG | G,W 604 | XP_005251175.1 | |
XM_006716700.1 | 2095 | Missense Mutation | GGG,TGG | G,W 777 | XP_006716763.1 | |
XM_006716701.1 | 2095 | Missense Mutation | GGG,TGG | G,W 774 | XP_006716764.1 | |
XM_006716702.1 | 2095 | Missense Mutation | GGG,TGG | G,W 761 | XP_006716765.1 | |
XM_006716703.1 | 2095 | Missense Mutation | GGG,TGG | G,W 696 | XP_006716766.1 | |
XM_006716704.1 | 2095 | Missense Mutation | GGG,TGG | G,W 668 | XP_006716767.1 | |
XM_006716705.1 | 2095 | Missense Mutation | GGG,TGG | G,W 652 | XP_006716768.1 | |
XM_006716706.1 | 2095 | Missense Mutation | GGG,TGG | G,W 587 | XP_006716769.1 | |
XM_011517403.1 | 2095 | Missense Mutation | GGG,TGG | G,W 711 | XP_011515705.1 | |
XM_011517404.2 | 2095 | Missense Mutation | GGG,TGG | G,W 697 | XP_011515706.1 | |
XM_011517407.1 | 2095 | Missense Mutation | GGG,TGG | G,W 420 | XP_011515709.1 | |
XM_017014086.1 | 2095 | Missense Mutation | GGG,TGG | G,W 773 | XP_016869575.1 | |
XM_017014087.1 | 2095 | Missense Mutation | GGG,TGG | G,W 753 | XP_016869576.1 | |
XM_017014088.1 | 2095 | Missense Mutation | GGG,TGG | G,W 749 | XP_016869577.1 | |
XM_017014089.1 | 2095 | Missense Mutation | GGG,TGG | G,W 748 | XP_016869578.1 | |
XM_017014090.1 | 2095 | Missense Mutation | GGG,TGG | G,W 723 | XP_016869579.1 | |
XM_017014091.1 | 2095 | Missense Mutation | GGG,TGG | G,W 715 | XP_016869580.1 | |
XM_017014092.1 | 2095 | Missense Mutation | GGG,TGG | G,W 709 | XP_016869581.1 | |
XM_017014093.1 | 2095 | Missense Mutation | GGG,TGG | G,W 664 | XP_016869582.1 | |
XM_017014094.1 | 2095 | Missense Mutation | GGG,TGG | G,W 648 | XP_016869583.1 | |
XM_017014095.1 | 2095 | Missense Mutation | GGG,TGG | G,W 644 | XP_016869584.1 | |
XM_017014096.1 | 2095 | Missense Mutation | GGG,TGG | G,W 643 | XP_016869585.1 | |
XM_017014097.1 | 2095 | Missense Mutation | GGG,TGG | G,W 639 | XP_016869586.1 | |
XM_017014098.1 | 2095 | Missense Mutation | GGG,TGG | G,W 600 | XP_016869587.1 | |
XM_017014099.1 | 2095 | Missense Mutation | GGG,TGG | G,W 599 | XP_016869588.1 | |
XM_017014100.1 | 2095 | Missense Mutation | GGG,TGG | G,W 583 | XP_016869589.1 | |
XM_017014101.1 | 2095 | Missense Mutation | GGG,TGG | G,W 559 | XP_016869590.1 |
NDUFB9 - NADH:ubiquinone oxidoreductase subunit B9 | ||||||
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There are no transcripts associated with this gene. |