Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACAGTCAATGCAGTCAACATTGGAT[C/G]GATTCATACCATATAAAGGCTGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 608187 | ||||||||||||||||||||
Literature Links: |
MCM8 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
MCM8 - minichromosome maintenance 8 homologous recombination repair factor | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281520.1 | 588 | Missense Mutation | CGA,GGA | R,G 71 | NP_001268449.1 | |
NM_001281521.1 | 588 | Missense Mutation | CGA,GGA | R,G 71 | NP_001268450.1 | |
NM_001281522.1 | 588 | Missense Mutation | CGA,GGA | R,G 71 | NP_001268451.1 | |
NM_032485.5 | 588 | Missense Mutation | CGA,GGA | R,G 71 | NP_115874.3 | |
NM_182802.2 | 588 | Missense Mutation | CGA,GGA | R,G 71 | NP_877954.1 | |
XM_011529387.2 | 588 | Missense Mutation | CGA,GGA | R,G 71 | XP_011527689.1 | |
XM_017028105.1 | 588 | Missense Mutation | CGA,GGA | R,G 71 | XP_016883594.1 | |
XM_017028106.1 | 588 | Missense Mutation | CGA,GGA | R,G 7 | XP_016883595.1 | |
XM_017028107.1 | 588 | Intron | XP_016883596.1 |
TRMT6 - tRNA methyltransferase 6 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |