Search Thermo Fisher Scientific
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GCCCAGTCCGTGTTGTCCGAAGTGC[A/C]CTCGGTGCCAACCAACGTGAGTGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300164 MIM: 314370 | ||||||||||||||||||||
Literature Links: |
INE1 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 |
INE1 - inactivation escape 1 (non-protein coding) | ||||||
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There are no transcripts associated with this gene. |
UBA1 - ubiquitin like modifier activating enzyme 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003334.3 | 209 | Missense Mutation | CAC,CCC | H,P 34 | NP_003325.2 | |
NM_153280.2 | 209 | Missense Mutation | CAC,CCC | H,P 34 | NP_695012.1 | |
XM_005272649.1 | 209 | Missense Mutation | CAC,CCC | H,P 40 | XP_005272706.1 | |
XM_011543954.2 | 209 | Missense Mutation | CAC,CCC | H,P 48 | XP_011542256.1 | |
XM_017029777.1 | 209 | Missense Mutation | CAC,CCC | H,P 85 | XP_016885266.1 | |
XM_017029778.1 | 209 | Missense Mutation | CAC,CCC | H,P 62 | XP_016885267.1 | |
XM_017029779.1 | 209 | Missense Mutation | CAC,CCC | H,P 40 | XP_016885268.1 | |
XM_017029780.1 | 209 | Missense Mutation | CAC,CCC | H,P 34 | XP_016885269.1 | |
XM_017029781.1 | 209 | Missense Mutation | CAC,CCC | H,P 34 | XP_016885270.1 |