Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611221 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GSDMB 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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GSDMB - gasdermin B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042471.1 | 2932 | Missense Mutation | AGG,GGG | R,G 291 | NP_001035936.1 | |
NM_001165958.1 | 2932 | Missense Mutation | AGG,GGG | R,G 304 | NP_001159430.1 | |
NM_001165959.1 | 2932 | Missense Mutation | AGG,GGG | R,G 295 | NP_001159431.1 | |
NM_018530.2 | 2932 | Missense Mutation | AGG,GGG | R,G 282 | NP_061000.2 | |
XM_011525004.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523306.1 | |
XM_011525006.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523308.1 | |
XM_011525007.2 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523309.1 | |
XM_011525009.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523311.1 | |
XM_011525011.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523313.1 | |
XM_011525012.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523314.1 | |
XM_011525013.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523315.1 | |
XM_011525015.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_011523317.1 | |
XM_017024848.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_016880337.1 | |
XM_017024849.1 | 2932 | Missense Mutation | AGG,GGG | R,G 308 | XP_016880338.1 | |
XM_017024850.1 | 2932 | Missense Mutation | AGG,GGG | R,G 304 | XP_016880339.1 | |
XM_017024851.1 | 2932 | Missense Mutation | AGG,GGG | R,G 299 | XP_016880340.1 | |
XM_017024852.1 | 2932 | Missense Mutation | AGG,GGG | R,G 291 | XP_016880341.1 | |
XM_017024853.1 | 2932 | Intron | XP_016880342.1 | |||
XM_017024854.1 | 2932 | Intron | XP_016880343.1 |