Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGACAACAACATACAGCGCACAG[A/G]GAATTCGTGCCTCAGGGTCATAGTC
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 |
---|---|---|
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 |
GSDMB - gasdermin B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042471.1 | 3203 | Missense Mutation | CCC,CTC | P,L 381 | NP_001035936.1 | |
NM_001165958.1 | 3203 | Missense Mutation | CCC,CTC | P,L 394 | NP_001159430.1 | |
NM_001165959.1 | 3203 | Missense Mutation | CCC,CTC | P,L 385 | NP_001159431.1 | |
NM_018530.2 | 3203 | Missense Mutation | CCC,CTC | P,L 372 | NP_061000.2 | |
XM_011525004.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523306.1 | |
XM_011525006.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523308.1 | |
XM_011525007.2 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523309.1 | |
XM_011525009.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523311.1 | |
XM_011525011.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523313.1 | |
XM_011525012.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523314.1 | |
XM_011525013.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523315.1 | |
XM_011525015.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_011523317.1 | |
XM_017024848.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_016880337.1 | |
XM_017024849.1 | 3203 | Missense Mutation | CCC,CTC | P,L 398 | XP_016880338.1 | |
XM_017024850.1 | 3203 | Missense Mutation | CCC,CTC | P,L 394 | XP_016880339.1 | |
XM_017024851.1 | 3203 | Missense Mutation | CCC,CTC | P,L 389 | XP_016880340.1 | |
XM_017024852.1 | 3203 | Missense Mutation | CCC,CTC | P,L 381 | XP_016880341.1 | |
XM_017024853.1 | 3203 | Intron | XP_016880342.1 | |||
XM_017024854.1 | 3203 | Intron | XP_016880343.1 |