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AGACAGCAAAAGCCTCCCCTTCGGG[C/G]CAGAACATTTCTTACATCCATTCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606622 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SMARCAL1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SMARCAL1 - SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127207.1 | 747 | Silent Mutation | GGC,GGG | G,G 201 | NP_001120679.1 | |
NM_014140.3 | 747 | Silent Mutation | GGC,GGG | G,G 201 | NP_054859.2 | |
XM_005246631.2 | 747 | Silent Mutation | GGC,GGG | G,G 201 | XP_005246688.1 | |
XM_005246632.1 | 747 | Silent Mutation | GGC,GGG | G,G 201 | XP_005246689.1 | |
XM_017004228.1 | 747 | UTR 5 | XP_016859717.1 |