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AGGATGCTGAACAGCAGTTTTGAGG[A/G]TGACCCCTTCTTCTCGTGAGTTACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601402 | ||||||||||||||||||||
Literature Links: |
LOC100996447 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 |
LOC100996447 - uncharacterized LOC100996447 | ||||||
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There are no transcripts associated with this gene. |
MLF1 - myeloid leukemia factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130156.2 | 169 | UTR 5 | NP_001123628.1 | |||
NM_001130157.2 | 169 | UTR 5 | NP_001123629.1 | |||
NM_001195432.1 | 169 | UTR 5 | NP_001182361.1 | |||
NM_001195433.1 | 169 | UTR 5 | NP_001182362.1 | |||
NM_001195434.1 | 169 | UTR 5 | NP_001182363.1 | |||
NM_022443.4 | 169 | Missense Mutation | GAT,GGT | D,G 11 | NP_071888.1 | |
XM_005247479.4 | 169 | Missense Mutation | GAT,GGT | D,G 11 | XP_005247536.1 | |
XM_005247480.2 | 169 | UTR 5 | XP_005247537.1 | |||
XM_006713645.2 | 169 | Missense Mutation | ATG,GTG | M,V 1 | XP_006713708.1 | |
XM_011512852.2 | 169 | UTR 5 | XP_011511154.1 | |||
XM_011512853.2 | 169 | UTR 5 | XP_011511155.1 | |||
XM_011512854.2 | 169 | UTR 5 | XP_011511156.1 |