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CCATTGGTGCTGTATCGTTTTGCAA[C/T]TGAATTCACAGCCTGGGGACTCAAC
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 |
---|---|---|
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 |
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 | 488 | Missense Mutation | ATT,GTT | I,V 144 | NP_001243820.1 | |
NM_001256892.1 | 488 | Missense Mutation | ATT,GTT | I,V 129 | NP_001243821.1 | |
NM_003130.3 | 488 | Missense Mutation | ATT,GTT | I,V 144 | NP_003121.1 | |
NM_198901.1 | 488 | Missense Mutation | ATT,GTT | I,V 129 | NP_944490.1 | |
XM_011516528.1 | 488 | Missense Mutation | ATT,GTT | I,V 101 | XP_011514830.1 |