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GAACCCAGCAAAATGGGGATCTCCA[A/C]AGTCATCCTTGAAATGTGTCTTTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601969 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DMBT1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
DMBT1 - deleted in malignant brain tumors 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320644.1 | 108 | Missense Mutation | AAA,ACA | K,T 5 | NP_001307573.1 | |
NM_004406.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | NP_004397.2 | |
NM_007329.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | NP_015568.2 | |
NM_017579.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | NP_060049.2 | |
XM_006717660.3 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_006717723.1 | |
XM_006717665.3 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_006717728.1 | |
XM_011539388.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537690.1 | |
XM_011539389.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537691.1 | |
XM_011539390.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537692.1 | |
XM_011539391.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537693.1 | |
XM_011539392.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537694.1 | |
XM_011539393.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537695.1 | |
XM_011539394.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537696.1 | |
XM_011539395.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537697.1 | |
XM_011539396.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537698.1 | |
XM_011539398.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537700.1 | |
XM_011539399.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537701.1 | |
XM_011539400.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537702.1 | |
XM_011539401.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537703.1 | |
XM_011539402.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537704.1 | |
XM_011539403.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537705.1 | |
XM_011539405.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537707.1 | |
XM_011539407.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537709.1 | |
XM_011539408.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537710.1 | |
XM_011539409.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537711.1 | |
XM_011539410.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537712.1 | |
XM_011539411.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537713.1 | |
XM_011539413.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537715.1 | |
XM_011539414.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537716.1 | |
XM_011539415.2 | 108 | Missense Mutation | AAA,ACA | K,T 5 | XP_011537717.1 | |
XM_017015798.1 | 108 | Intron | XP_016871287.1 |