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AGGAGTGGCAGATGTGGACATGTCC[C/T]GGGATAGCTGCATTGGTGTTGATGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606365 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GLS2 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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GLS2 - glutaminase 2 | ||||||
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There are no transcripts associated with this gene. |
SPRYD4 - SPRY domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_207344.3 | 406 | Missense Mutation | CGG,TGG | R,W 111 | NP_997227.1 |