Search Thermo Fisher Scientific
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AAGCATCACAGTGGGGCCCAGCAGC[C/T]GTGCCTTCTTGGCCCTCCTCCGCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611340 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATG4D 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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ATG4D - autophagy related 4D cysteine peptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281504.1 | 1994 | Intron | NP_001268433.1 | |||
NM_032885.5 | 1994 | Intron | NP_116274.3 | |||
XM_006722927.1 | 1994 | Intron | XP_006722990.1 |
KRI1 - KRI1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023008.3 | 1994 | Missense Mutation | CAG,CGG | Q,R 662 | NP_075384.3 | |
XM_011528190.2 | 1994 | Missense Mutation | CAG,CGG | Q,R 544 | XP_011526492.1 |
MIR1238 - microRNA 1238 | ||||||
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There are no transcripts associated with this gene. |