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ACTATAGGCAGCAAATAACAGGTTG[A/G]CCACAGTCTTGTTCTGGAACACAAA
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 |
---|---|---|
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 |
GLS2 - glutaminase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001280796.1 | 1629 | Missense Mutation | GCC,GTC | A,V 212 | NP_001267725.1 | |
NM_001280797.1 | 1629 | Missense Mutation | GCC,GTC | A,V 223 | NP_001267726.1 | |
NM_001280798.1 | 1629 | Missense Mutation | GCC,GTC | A,V 223 | NP_001267727.1 | |
NM_013267.3 | 1629 | Missense Mutation | GCC,GTC | A,V 488 | NP_037399.2 | |
XM_005268797.1 | 1629 | Missense Mutation | GCC,GTC | A,V 452 | XP_005268854.1 | |
XM_017019180.1 | 1629 | Missense Mutation | GCC,GTC | A,V 223 | XP_016874669.1 |
SPRYD4 - SPRY domain containing 4 | ||||||
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There are no transcripts associated with this gene. |