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AGCTGCATTTCAGGAGGCATATTAG[A/G]GATCTCTTCTCCACTTACAGTTATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 601749 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C1orf146 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C1orf146 - chromosome 1 open reading frame 146 | ||||||
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There are no transcripts associated with this gene. |
GLMN - glomulin, FKBP associated protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319683.1 | 1640 | Missense Mutation | CCT,TCT | P,S 533 | NP_001306612.1 | |
NM_053274.2 | 1640 | Missense Mutation | CCT,TCT | P,S 547 | NP_444504.1 | |
XM_005270401.3 | 1640 | Missense Mutation | CCT,TCT | P,S 505 | XP_005270458.1 | |
XM_006710309.2 | 1640 | Missense Mutation | CCT,TCT | P,S 380 | XP_006710372.1 | |
XM_011540546.2 | 1640 | Missense Mutation | CCT,TCT | P,S 547 | XP_011538848.1 | |
XM_017000137.1 | 1640 | Missense Mutation | CCT,TCT | P,S 580 | XP_016855626.1 | |
XM_017000138.1 | 1640 | Missense Mutation | CCT,TCT | P,S 566 | XP_016855627.1 | |
XM_017000139.1 | 1640 | Missense Mutation | CCT,TCT | P,S 545 | XP_016855628.1 | |
XM_017000140.1 | 1640 | Missense Mutation | CCT,TCT | P,S 538 | XP_016855629.1 | |
XM_017000141.1 | 1640 | Missense Mutation | CCT,TCT | P,S 512 | XP_016855630.1 | |
XM_017000142.1 | 1640 | Missense Mutation | CCT,TCT | P,S 366 | XP_016855631.1 | |
XM_017000143.1 | 1640 | Missense Mutation | CCT,TCT | P,S 366 | XP_016855632.1 | |
XM_017000144.1 | 1640 | Missense Mutation | CCT,TCT | P,S 290 | XP_016855633.1 |