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ATATAGATCTTGGTTAGACATGGAG[A/G]AGGACTTCCCAAGACAGGAATAAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
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Literature Links: |
C1orf61 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 |
C1orf61 - chromosome 1 open reading frame 61 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320453.1 | 707 | Intron | NP_001307382.1 | |||
NM_001320454.1 | 707 | Intron | NP_001307383.1 | |||
NM_001320455.1 | 707 | Intron | NP_001307384.1 | |||
NM_006365.2 | 707 | Missense Mutation | TCC,TTC | S,F 116 | NP_006356.1 | |
XM_011509067.1 | 707 | Intron | XP_011507369.1 | |||
XM_011509068.1 | 707 | Intron | XP_011507370.1 | |||
XM_011509070.1 | 707 | Missense Mutation | TCC,TTC | S,F 116 | XP_011507372.1 | |
XM_011509071.2 | 707 | Missense Mutation | TCC,TTC | S,F 116 | XP_011507373.1 | |
XM_011509072.1 | 707 | Missense Mutation | TCC,TTC | S,F 116 | XP_011507374.1 | |
XM_011509073.2 | 707 | Missense Mutation | TCC,TTC | S,F 102 | XP_011507375.1 | |
XM_011509074.1 | 707 | Missense Mutation | TCC,TTC | S,F 99 | XP_011507376.1 | |
XM_017000061.1 | 707 | Intron | XP_016855550.1 | |||
XM_017000062.1 | 707 | Missense Mutation | TCC,TTC | S,F 116 | XP_016855551.1 | |
XM_017000063.1 | 707 | Missense Mutation | TCC,TTC | S,F 116 | XP_016855552.1 | |
XM_017000064.1 | 707 | Intron | XP_016855553.1 | |||
XM_017000065.1 | 707 | Intron | XP_016855554.1 | |||
XM_017000066.1 | 707 | Intron | XP_016855555.1 |