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TTCTTGTGGGTCTACTGTTCCACTC[C/G]TGTCAGTGTCAAAACTGATAAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603709 MIM: 182520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ADAM22 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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ADAM22 - ADAM metallopeptidase domain 22 | ||||||
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There are no transcripts associated with this gene. |
LOC102723885 - uncharacterized LOC102723885 | ||||||
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There are no transcripts associated with this gene. |
SRI - sorcin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256891.1 | 405 | Missense Mutation | ACG,AGG | T,R 116 | NP_001243820.1 | |
NM_001256892.1 | 405 | Missense Mutation | ACG,AGG | T,R 101 | NP_001243821.1 | |
NM_003130.3 | 405 | Missense Mutation | ACG,AGG | T,R 116 | NP_003121.1 | |
NM_198901.1 | 405 | Missense Mutation | ACG,AGG | T,R 101 | NP_944490.1 | |
XM_011516528.1 | 405 | Missense Mutation | ACG,AGG | T,R 73 | XP_011514830.1 |