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GACCTCGGGGCCGACCAAAGGGAAG[C/T]AAAAACAAGGGTGCTGCCAAGACCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611419 MIM: 600701 | ||||||||||||||||||||
Literature Links: |
C6orf1 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 |
C6orf1 - chromosome 6 open reading frame 1 | ||||||
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There are no transcripts associated with this gene. |
HMGA1 - high mobility group AT-hook 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319077.1 | 648 | Silent Mutation | AGC,AGT | S,S 53 | NP_001306006.1 | |
NM_001319078.1 | 648 | Intron | NP_001306007.1 | |||
NM_001319079.1 | 648 | Silent Mutation | AGC,AGT | S,S 64 | NP_001306008.1 | |
NM_001319080.1 | 648 | Silent Mutation | AGC,AGT | S,S 63 | NP_001306009.1 | |
NM_001319081.1 | 648 | Intron | NP_001306010.1 | |||
NM_001319082.1 | 648 | Silent Mutation | AGC,AGT | S,S 64 | NP_001306011.1 | |
NM_002131.3 | 648 | Silent Mutation | AGC,AGT | S,S 53 | NP_002122.1 | |
NM_145899.2 | 648 | Silent Mutation | AGC,AGT | S,S 64 | NP_665906.1 | |
NM_145901.2 | 648 | Silent Mutation | AGC,AGT | S,S 64 | NP_665908.1 | |
NM_145902.2 | 648 | Silent Mutation | AGC,AGT | S,S 53 | NP_665909.1 | |
NM_145903.2 | 648 | Intron | NP_665910.1 | |||
NM_145905.2 | 648 | Intron | NP_665912.1 |
MIR6835 - microRNA 6835 | ||||||
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There are no transcripts associated with this gene. |