Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCATCAACTGAATCTCACTGACCA[G/C]AGGGACTGTGGTGATCACAACTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616334 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TMEM100 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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TMEM100 - transmembrane protein 100 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099640.1 | 2272 | Missense Mutation | CTG,GTG | L,V 36 | NP_001093110.1 | |
NM_018286.2 | 2272 | Missense Mutation | CTG,GTG | L,V 36 | NP_060756.2 | |
XM_017024814.1 | 2272 | Missense Mutation | CTG,GTG | L,V 36 | XP_016880303.1 | |
XM_017024815.1 | 2272 | Missense Mutation | CTG,GTG | L,V 36 | XP_016880304.1 | |
XM_017024816.1 | 2272 | Missense Mutation | CTG,GTG | L,V 36 | XP_016880305.1 |