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ACTTGGGGGACCCAGCGAAATGGAA[C/G]AAGTTAGGTGTCCAGAGCACGGTAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
MIM: 604718 | ||||||||||||||||||||
Literature Links: |
LOC101929099 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 |
LOC101929099 - uncharacterized LOC101929099 | ||||||
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There are no transcripts associated with this gene. |
TTF2 - transcription termination factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003594.3 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | NP_003585.3 | |
XM_005271277.3 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_005271334.1 | |
XM_011542303.2 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_011540605.1 | |
XM_017002549.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858038.1 | |
XM_017002550.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858039.1 | |
XM_017002551.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858040.1 | |
XM_017002552.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858041.1 | |
XM_017002553.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858042.1 | |
XM_017002554.1 | 66 | Missense Mutation | CAA,GAA | Q,E 3 | XP_016858043.1 | |
XM_017002555.1 | 66 | Nonsense Mutation | CAA,GAA | Q,E 3 | XP_016858044.1 |