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GCCAAAGGACCCTGGAAGAAGGGGC[A/G]GTTGAGGAGTTCATGTTCCAGCTCT
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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
ACTN1 - actinin alpha 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102.3 | Intron | NP_001093.1 | ||||
NM_001130004.1 | Intron | NP_001123476.1 | ||||
NM_001130005.1 | Intron | NP_001123477.1 | ||||
XM_011537265.2 | Intron | XP_011535567.1 | ||||
XM_011537266.2 | Intron | XP_011535568.1 | ||||
XM_011537267.2 | Intron | XP_011535569.1 | ||||
XM_011537268.2 | Intron | XP_011535570.1 | ||||
XM_017021720.1 | Intron | XP_016877209.1 | ||||
XM_017021721.1 | Intron | XP_016877210.1 | ||||
XM_017021722.1 | Intron | XP_016877211.1 | ||||
XM_017021723.1 | Intron | XP_016877212.1 | ||||
XM_017021725.1 | Intron | XP_016877214.1 | ||||
XM_017021726.1 | Intron | XP_016877215.1 | ||||
XM_017021727.1 | Intron | XP_016877216.1 | ||||
XM_017021728.1 | Intron | XP_016877217.1 |