Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGCCCAAGCCCTGGTGTGCCGGC[A/C]CCTAGGCCGAGGTGAGTCACAGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611338 | ||||||||||||||||||||
Literature Links: |
ATG4B 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 |
ATG4B - autophagy related 4B cysteine peptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013325.4 | 474 | Missense Mutation | CAC,CCC | H,P 91 | NP_037457.3 | |
NM_178326.2 | 474 | Missense Mutation | CAC,CCC | H,P 91 | NP_847896.1 | |
XM_005246992.3 | 474 | Missense Mutation | CAC,CCC | H,P 91 | XP_005247049.2 | |
XM_005246993.2 | 474 | Missense Mutation | CAC,CCC | H,P 91 | XP_005247050.2 | |
XM_005246995.3 | 474 | Missense Mutation | CAC,CCC | H,P 17 | XP_005247052.1 | |
XM_005246996.2 | 474 | Missense Mutation | CAC,CCC | H,P 17 | XP_005247053.1 | |
XM_017003637.1 | 474 | Missense Mutation | CAC,CCC | H,P 155 | XP_016859126.1 | |
XM_017003638.1 | 474 | Missense Mutation | CAC,CCC | H,P 155 | XP_016859127.1 | |
XM_017003639.1 | 474 | Missense Mutation | CAC,CCC | H,P 17 | XP_016859128.1 | |
XM_017003640.1 | 474 | Missense Mutation | CAC,CCC | H,P 17 | XP_016859129.1 |