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GGCGCTGGGCAGCCTGTTGGTGCTG[A/T]TGGTGCTGCACTCGCCGTCGCTGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612200 | ||||||||||||||||||||
Literature Links: |
C3orf58 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 |
C3orf58 - chromosome 3 open reading frame 58 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134470.1 | 617 | Intron | NP_001127942.1 | |||
NM_173552.3 | 617 | Missense Mutation | ATG,TTG | M,L 28 | NP_775823.1 | |
XM_011512543.2 | 617 | Missense Mutation | ATG,TTG | M,L 28 | XP_011510845.1 | |
XM_017005869.1 | 617 | Intron | XP_016861358.1 |