Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGACCTCAGTAATTTTGGCCTCAG[C/T]TGATCCTCTAAAAACAAAACACAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609175 MIM: 605273 | ||||||||||||||||||||
Literature Links: |
DSN1 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 |
DSN1 - DSN1 homolog, MIS12 kinetochore complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145315.1 | 1088 | Missense Mutation | ACT,GCT | T,A 245 | NP_001138787.1 | |
NM_001145316.1 | 1088 | Missense Mutation | ACT,GCT | T,A 245 | NP_001138788.1 | |
NM_001145317.1 | 1088 | Missense Mutation | ACT,GCT | T,A 138 | NP_001138789.1 | |
NM_001145318.1 | 1088 | Missense Mutation | ACT,GCT | T,A 229 | NP_001138790.1 | |
NM_024918.3 | 1088 | Missense Mutation | ACT,GCT | T,A 245 | NP_079194.3 | |
XM_006723876.2 | 1088 | Missense Mutation | ACT,GCT | T,A 138 | XP_006723939.1 | |
XM_017028070.1 | 1088 | Missense Mutation | ACT,GCT | T,A 233 | XP_016883559.1 | |
XM_017028071.1 | 1088 | Missense Mutation | ACT,GCT | T,A 233 | XP_016883560.1 | |
XM_017028072.1 | 1088 | Missense Mutation | ACT,GCT | T,A 217 | XP_016883561.1 |
NDRG3 - NDRG family member 3 | ||||||
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There are no transcripts associated with this gene. |