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AGAGAGGCCAGGGAATGCTCAGAGG[G/T]CCGCCTTCGGGGCATCCATGTAGGC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606605 MIM: 607290 MIM: 606609 | |||||||||||||||||||||||
Literature Links: |
ATRIP 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 - 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 |
ATRIP - ATR interacting protein | ||||||
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There are no transcripts associated with this gene. |
SHISA5 - shisa family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272065.1 | 1032 | Intron | NP_001258994.1 | |||
NM_001272066.1 | 1032 | Missense Mutation | NP_001258995.1 | |||
NM_001272067.1 | 1032 | Missense Mutation | NP_001258996.1 | |||
NM_001272068.1 | 1032 | Missense Mutation | NP_001258997.1 | |||
NM_001272082.1 | 1032 | Missense Mutation | NP_001259011.1 | |||
NM_001272083.1 | 1032 | UTR 3 | NP_001259012.1 | |||
NM_016479.4 | 1032 | Intron | NP_057563.3 | |||
XM_005265205.1 | 1032 | Missense Mutation | XP_005265262.1 | |||
XM_006713188.2 | 1032 | Missense Mutation | XP_006713251.1 | |||
XM_011533796.1 | 1032 | Missense Mutation | XP_011532098.1 |
TREX1 - three prime repair exonuclease 1 | ||||||
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There are no transcripts associated with this gene. |