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TGAAGATGATCTTGTAAAGGAAAGT[C/T]CTAGTTGTGGGAAAGACACTCCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603514 | ||||||||||||||||||||
Literature Links: |
FAM210A 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 |
FAM210A - family with sequence similarity 210 member A | ||||||
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There are no transcripts associated with this gene. |
RNMT - RNA guanine-7 methyltransferase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308263.1 | 452 | Missense Mutation | CCT,TCT | P,S 71 | NP_001295192.1 | |
NM_003799.2 | 452 | Missense Mutation | CCT,TCT | P,S 71 | NP_003790.1 | |
XM_005258162.1 | 452 | Missense Mutation | CCT,TCT | P,S 71 | XP_005258219.1 | |
XM_011525749.1 | 452 | Missense Mutation | CCT,TCT | P,S 71 | XP_011524051.1 | |
XM_011525750.2 | 452 | Missense Mutation | CCT,TCT | P,S 71 | XP_011524052.1 | |
XM_011525751.1 | 452 | Missense Mutation | CCT,TCT | P,S 71 | XP_011524053.1 | |
XM_011525753.1 | 452 | Intron | XP_011524055.1 | |||
XM_017026061.1 | 452 | Missense Mutation | CCT,TCT | P,S 71 | XP_016881550.1 |