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CCATTAGTTGTGAGGGACATGCAAA[C/T]GAAGACCATAAGAAGATGCGATTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603254 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMARCA4 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
|
SMARCA4 - SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128844.1 | Intron | NP_001122316.1 | ||||
NM_001128845.1 | Intron | NP_001122317.1 | ||||
NM_001128846.1 | Intron | NP_001122318.1 | ||||
NM_001128847.1 | Intron | NP_001122319.1 | ||||
NM_001128848.1 | Intron | NP_001122320.1 | ||||
NM_001128849.1 | Intron | NP_001122321.1 | ||||
NM_003072.3 | Intron | NP_003063.2 | ||||
XM_006722845.2 | Intron | XP_006722908.1 | ||||
XM_006722846.2 | Intron | XP_006722909.1 | ||||
XM_011528198.1 | Intron | XP_011526500.1 | ||||
XM_017027160.1 | Intron | XP_016882649.1 | ||||
XM_017027161.1 | Intron | XP_016882650.1 | ||||
XM_017027162.1 | Intron | XP_016882651.1 | ||||
XM_017027163.1 | Intron | XP_016882652.1 | ||||
XM_017027164.1 | Intron | XP_016882653.1 | ||||
XM_017027165.1 | Intron | XP_016882654.1 | ||||
XM_017027166.1 | Intron | XP_016882655.1 | ||||
XM_017027167.1 | Intron | XP_016882656.1 | ||||
XM_017027168.1 | Intron | XP_016882657.1 |