Product Details
- SNP ID
-
rs189973248
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:122560796 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATGGGGATCTCCACAGTCATCCTTG[A/G]AATGTGTCTTTTATGGGGACAAGTT
- Phenotype
-
MIM: 601969
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DMBT1
PubMed Links
Gene Details
- Gene
- DMBT1
- Gene Name
- deleted in malignant brain tumors 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001320644.1 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
NP_001307573.1 |
NM_004406.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
NP_004397.2 |
NM_007329.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
NP_015568.2 |
NM_017579.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
NP_060049.2 |
XM_006717660.3 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_006717723.1 |
XM_006717665.3 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_006717728.1 |
XM_011539388.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537690.1 |
XM_011539389.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537691.1 |
XM_011539390.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537692.1 |
XM_011539391.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537693.1 |
XM_011539392.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537694.1 |
XM_011539393.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537695.1 |
XM_011539394.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537696.1 |
XM_011539395.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537697.1 |
XM_011539396.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537698.1 |
XM_011539398.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537700.1 |
XM_011539399.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537701.1 |
XM_011539400.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537702.1 |
XM_011539401.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537703.1 |
XM_011539402.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537704.1 |
XM_011539403.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537705.1 |
XM_011539405.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537707.1 |
XM_011539407.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537709.1 |
XM_011539408.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537710.1 |
XM_011539409.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537711.1 |
XM_011539410.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537712.1 |
XM_011539411.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537713.1 |
XM_011539413.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537715.1 |
XM_011539414.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537716.1 |
XM_011539415.2 |
120 |
Missense Mutation |
GAA,GGA |
E9G |
XP_011537717.1 |
XM_017015798.1 |
120 |
Intron |
|
|
XP_016871287.1 |
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