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GCAGTTGCTTGGATTGTTGATTTCC[C/T]TCATTCTTTGTAGACTCATCTCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616226 MIM: 616605 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATG2B 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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ATG2B - autophagy related 2B | ||||||
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There are no transcripts associated with this gene. |
GSKIP - GSK3B interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271904.1 | Intron | NP_001258833.1 | ||||
NM_001271905.1 | Intron | NP_001258834.1 | ||||
NM_001271906.1 | Intron | NP_001258835.1 | ||||
NM_016472.4 | Intron | NP_057556.2 | ||||
XM_017021365.1 | Intron | XP_016876854.1 |