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TCAAGCACCGGGGCGGGGATCTCTC[C/T]GTAAGACGAGACCTCTGGTTGTGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603801 MIM: 606116 | ||||||||||||||||||||
Literature Links: |
C10orf111 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 |
C10orf111 - chromosome 10 open reading frame 111 | ||||||
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There are no transcripts associated with this gene. |
NMT2 - N-myristoyltransferase 2 | ||||||
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There are no transcripts associated with this gene. |
RPP38 - ribonuclease P/MRP subunit p38 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001097590.2 | 280 | Missense Mutation | CGT,TGT | R,C 14 | NP_001091059.1 | |
NM_001265601.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | NP_001252530.1 | |
NM_006414.4 | 280 | Missense Mutation | CGT,TGT | R,C 14 | NP_006405.2 | |
NM_183005.4 | 280 | Missense Mutation | CGT,TGT | R,C 14 | NP_892117.1 | |
XM_006717363.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_006717426.1 | |
XM_006717364.3 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_006717427.1 | |
XM_011519293.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_011517595.1 | |
XM_017015479.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_016870968.1 | |
XM_017015480.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_016870969.1 | |
XM_017015481.1 | 280 | Missense Mutation | CGT,TGT | R,C 14 | XP_016870970.1 |