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TACCTTATCTTCAACACTTTCTTTA[A/C]TGTGTGAAAGATGCTCTAATTCTTT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611965 | |||||||||||||||||||||||
Literature Links: |
C3orf49 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 |
C3orf49 - chromosome 3 open reading frame 49 | ||||||
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There are no transcripts associated with this gene. |
THOC7 - THO complex 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001285387.2 | 537 | Missense Mutation | AGT,ATT | S,I 100 | NP_001272316.1 | |
NM_001285404.1 | 537 | Missense Mutation | AGT,ATT | S,I 100 | NP_001272333.1 | |
NM_025075.3 | 537 | Missense Mutation | AGT,ATT | S,I 152 | NP_079351.2 | |
XM_006713339.3 | 537 | Missense Mutation | AGT,ATT | S,I 100 | XP_006713402.1 |