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- SNP ID:
- rs149781615
- Gene
-
FLJ21408NSMCE1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.16: 27268932 - 27268932 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
ATTACGCCCGCTCTCGATCCTTAAT[A/G]ATGGGAAGGGGCTTCCACTTGTCGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
FLJ21408 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
| FLJ21408 - uncharacterized LOC400512 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| NSMCE1 - NSE1 homolog, SMC5-SMC6 complex component | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_145080.3 | Intron | NP_659547.2 | ||||
| XM_006721023.3 | Intron | XP_006721086.1 | ||||
| XM_011545761.2 | Intron | XP_011544063.1 | ||||
| XM_011545762.1 | Intron | XP_011544064.1 | ||||
| XM_017023040.1 | Intron | XP_016878529.1 | ||||
| XM_017023041.1 | Intron | XP_016878530.1 | ||||
| XM_017023042.1 | Intron | XP_016878531.1 | ||||
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