Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGGCCGGTGTAGGGGGCCATCCGC[A/G]CGATGCAGTACTCAGCCTGGTCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 102575 | ||||||||||||||||||||
Literature Links: |
ACTN1 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 |
ACTN1 - actinin alpha 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102.3 | 3537 | Missense Mutation | GCG,GTG | A,V 862 | NP_001093.1 | |
NM_001130004.1 | 3537 | Missense Mutation | GCG,GTG | A,V 884 | NP_001123476.1 | |
NM_001130005.1 | 3537 | Missense Mutation | GCG,GTG | A,V 857 | NP_001123477.1 | |
XM_011537265.2 | 3537 | Missense Mutation | GCG,GTG | A,V 899 | XP_011535567.1 | |
XM_011537266.2 | 3537 | Missense Mutation | GCG,GTG | A,V 894 | XP_011535568.1 | |
XM_011537267.2 | 3537 | Missense Mutation | GCG,GTG | A,V 891 | XP_011535569.1 | |
XM_011537268.2 | 3537 | Missense Mutation | GCG,GTG | A,V 886 | XP_011535570.1 | |
XM_017021720.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1076 | XP_016877209.1 | |
XM_017021721.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1068 | XP_016877210.1 | |
XM_017021722.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1047 | XP_016877211.1 | |
XM_017021723.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1039 | XP_016877212.1 | |
XM_017021725.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1026 | XP_016877214.1 | |
XM_017021726.1 | 3537 | Missense Mutation | GCG,GTG | A,V 1018 | XP_016877215.1 | |
XM_017021727.1 | 3537 | Missense Mutation | GCG,GTG | A,V 865 | XP_016877216.1 | |
XM_017021728.1 | 3537 | Missense Mutation | GCG,GTG | A,V 836 | XP_016877217.1 |