Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCTTGCTCCTTAATTGCGATCCCC[C/T]ATCAGCTGCAGCACAAAGGTGAAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603488 MIM: 609023 MIM: 610364 | ||||||||||||||||||||
Literature Links: |
AAMP 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 |
AAMP - angio associated migratory cell protein | ||||||
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There are no transcripts associated with this gene. |
MIR6513 - microRNA 6513 | ||||||
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There are no transcripts associated with this gene. |
PNKD - paroxysmal nonkinesigenic dyskinesia | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077399.2 | 998 | Intron | NP_001070867.1 | |||
NM_015488.4 | 998 | Intron | NP_056303.3 | |||
NM_022572.4 | 998 | Intron | NP_072094.1 | |||
XM_017003771.1 | 998 | Intron | XP_016859260.1 | |||
XM_017003772.1 | 998 | Intron | XP_016859261.1 |
TMBIM1 - transmembrane BAX inhibitor motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321427.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308356.1 | |
NM_001321428.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308357.1 | |
NM_001321429.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308358.1 | |
NM_001321430.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308359.1 | |
NM_001321432.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308361.1 | |
NM_001321433.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308362.1 | |
NM_001321435.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308364.1 | |
NM_001321436.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_001308365.1 | |
NM_001321438.1 | 998 | Missense Mutation | ATA,ATG | I,M 196 | NP_001308367.1 | |
NM_022152.5 | 998 | Missense Mutation | ATA,ATG | I,M 307 | NP_071435.2 | |
XM_011511627.1 | 998 | Missense Mutation | ATA,ATG | I,M 307 | XP_011509929.1 |