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TCCTGCCGGGCTGGTCTCAAAGCAG[A/G]AGGCCGGACTGGTTGGAGAGATGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610454 MIM: 612971 | ||||||||||||||||||||
Literature Links: |
LZTS2 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 |
LZTS2 - leucine zipper tumor suppressor 2 | ||||||
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There are no transcripts associated with this gene. |
PDZD7 - PDZ domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195263.1 | 2164 | Missense Mutation | CCT,TCT | P,S 648 | NP_001182192.1 | |
NM_024895.4 | 2164 | Intron | NP_079171.1 | |||
XM_005270165.2 | 2164 | UTR 3 | XP_005270222.1 | |||
XM_011540177.2 | 2164 | Missense Mutation | CCT,TCT | P,S 648 | XP_011538479.1 | |
XM_011540178.2 | 2164 | Missense Mutation | CCT,TCT | P,S 647 | XP_011538480.1 | |
XM_011540179.2 | 2164 | Missense Mutation | CCT,TCT | P,S 648 | XP_011538481.1 | |
XM_011540181.2 | 2164 | Intron | XP_011538483.1 | |||
XM_011540182.2 | 2164 | Intron | XP_011538484.1 | |||
XM_011540183.2 | 2164 | Intron | XP_011538485.1 | |||
XM_017016667.1 | 2164 | Intron | XP_016872156.1 | |||
XM_017016668.1 | 2164 | Intron | XP_016872157.1 |