Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACGAGACACCCCTGAGCCGCGCGC[C/T]CCTAGCCCTCCGCACGCGCCACATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615549 | ||||||||||||||||||||
Literature Links: |
ARMC5 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 |
ARMC5 - armadillo repeat containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105247.1 | 793 | Missense Mutation | CCC,CTC | P,L 44 | NP_001098717.1 | |
NM_001288767.1 | 793 | Missense Mutation | CCC,CTC | P,L 139 | NP_001275696.1 | |
NM_001301820.1 | 793 | Missense Mutation | CCC,CTC | P,L 76 | NP_001288749.1 | |
NM_024742.2 | 793 | Missense Mutation | CCC,CTC | P,L 44 | NP_079018.1 | |
XM_006721091.2 | 793 | Missense Mutation | CCC,CTC | P,L 76 | XP_006721154.1 |