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- SNP ID:
- rs142248327
- Gene
-
FAM189A1NSMCE3 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.15: 29268759 - 29268759 on Build GRCh38
- Polymorphism:
- C/G, Transversion substitution
- Context Sequence [VIC/FAM]:
TAAACTGTGCCTTTGGGTCTCAGAC[C/G]CTTGTCCCGGGGGTCCCTCTGAATC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608243
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Literature Links: |
FAM189A1 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
|
| FAM189A1 - family with sequence similarity 189 member A1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015307.1 | 1058 | Intron | NP_056122.1 | |||
| XM_011521407.2 | 1058 | Intron | XP_011519709.1 | |||
| NSMCE3 - NSE3 homolog, SMC5-SMC6 complex component | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_138704.3 | 1058 | UTR 3 | NP_619649.1 | |||
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