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TCTTCTTCATCTAAAGATTCCACAG[C/T]ATTAGTGAAAAGTTTTCCAATACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609644 | ||||||||||||||||||||
Literature Links: |
FANCM 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 |
FANCM - Fanconi anemia complementation group M | ||||||
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There are no transcripts associated with this gene. |
MIS18BP1 - MIS18 binding protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018353.4 | 3824 | Missense Mutation | ACT,GCT | T,A 1113 | NP_060823.3 | |
XM_005267833.4 | 3824 | Missense Mutation | ACT,GCT | T,A 1113 | XP_005267890.1 | |
XM_011536923.1 | 3824 | Missense Mutation | ACT,GCT | T,A 725 | XP_011535225.1 | |
XM_017021425.1 | 3824 | Missense Mutation | ACT,GCT | T,A 1113 | XP_016876914.1 |