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GGCCCAAGCTCCGGCCCGGCCGGCC[A/G]CTGCGTTCGAAAGGTAGGACGCGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604573 | ||||||||||||||||||||
Literature Links: |
C14orf2 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 |
C14orf2 - chromosome 14 open reading frame 2 | ||||||
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There are no transcripts associated with this gene. |
TDRD9 - tudor domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153046.2 | 369 | Missense Mutation | ACT,GCT | T,A 68 | NP_694591.2 | |
XM_005267309.3 | 369 | Missense Mutation | ACT,GCT | T,A 68 | XP_005267366.1 | |
XM_006720019.3 | 369 | Missense Mutation | ACT,GCT | T,A 68 | XP_006720082.1 | |
XM_006720020.3 | 369 | Missense Mutation | ACT,GCT | T,A 68 | XP_006720083.1 | |
XM_011536397.2 | 369 | Missense Mutation | ACT,GCT | T,A 68 | XP_011534699.1 | |
XM_011536398.2 | 369 | Intron | XP_011534700.1 | |||
XM_011536400.2 | 369 | Missense Mutation | ACT,GCT | T,A 68 | XP_011534702.1 | |
XM_011536401.2 | 369 | Intron | XP_011534703.1 | |||
XM_011536402.2 | 369 | Intron | XP_011534704.1 | |||
XM_017020955.1 | 369 | UTR 5 | XP_016876444.1 |