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AGACCAGGAGGGAGAAGGAAAATGG[A/C]GAGTTTTACGAGCTTGCCAAGCTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600892 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SIM2 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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SIM2 - single-minded family bHLH transcription factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005069.4 | 684 | Silent Mutation | GGA,GGC | G,G 18 | NP_005060.1 | |
NM_009586.3 | 684 | Silent Mutation | GGA,GGC | G,G 18 | NP_033664.2 | |
XM_011529694.1 | 684 | Intron | XP_011527996.1 | |||
XM_017028442.1 | 684 | Silent Mutation | GGA,GGC | G,G 18 | XP_016883931.1 |