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AATAATTACCATTGTGCTGAAACTC[A/T]GGATCTCTAAGAGAGCCCTGAATTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613813 | ||||||||||||||||||||
Literature Links: |
MDM1 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 |
MDM1 - Mdm1 nuclear protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001205028.1 | 1984 | Silent Mutation | CCA,CCT | P,P 617 | NP_001191957.1 | |
NM_001205029.1 | 1984 | Intron | NP_001191958.1 | |||
NM_017440.4 | 1984 | Silent Mutation | CCA,CCT | P,P 652 | NP_059136.2 | |
NM_020128.2 | 1984 | Intron | NP_064513.1 | |||
XM_005269026.1 | 1984 | Silent Mutation | CCA,CCT | P,P 662 | XP_005269083.1 | |
XM_011538569.1 | 1984 | Intron | XP_011536871.1 | |||
XM_017019646.1 | 1984 | Silent Mutation | CCA,CCT | P,P 382 | XP_016875135.1 | |
XM_017019647.1 | 1984 | Silent Mutation | CCA,CCT | P,P 382 | XP_016875136.1 | |
XM_017019648.1 | 1984 | Silent Mutation | CCA,CCT | P,P 382 | XP_016875137.1 | |
XM_017019649.1 | 1984 | Silent Mutation | CCA,CCT | P,P 382 | XP_016875138.1 | |
XM_017019650.1 | 1984 | Silent Mutation | CCA,CCT | P,P 382 | XP_016875139.1 |