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CCAGCCGAACCCGCTCCAGGTTACC[G/T]CTATCGTCAAGTACTGGTATGCTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605143 MIM: 607035 | ||||||||||||||||||||
Literature Links: |
ACTR1A 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 |
ACTR1A - ARP1 actin-related protein 1 homolog A, centractin alpha | ||||||
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There are no transcripts associated with this gene. |
SUFU - SUFU negative regulator of hedgehog signaling | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178133.1 | 357 | Missense Mutation | GCT,TCT | A,S 56 | NP_001171604.1 | |
NM_016169.3 | 357 | Missense Mutation | GCT,TCT | A,S 56 | NP_057253.2 | |
XM_011539858.2 | 357 | Missense Mutation | GCT,TCT | A,S 56 | XP_011538160.1 | |
XM_011539860.2 | 357 | Missense Mutation | GCT,TCT | A,S 56 | XP_011538162.1 | |
XM_011539861.2 | 357 | Missense Mutation | GCT,TCT | A,S 56 | XP_011538163.1 | |
XM_011539863.2 | 357 | Intron | XP_011538165.1 | |||
XM_011539864.2 | 357 | Missense Mutation | GCT,TCT | A,S 56 | XP_011538166.1 | |
XM_017016323.1 | 357 | Intron | XP_016871812.1 |