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EMILIN2 (exon)
QuickView for rs149714951 (snp)
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Macaque
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Human
C|G
- Chimp
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Mouse
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Rat
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- Type:
- SNP
- Organism:
- Homo sapiens
- Alleles:
- C|G
- Chromosomal Location:
- chr 18 : 2881300 (build 36.3)
- Strand:
- +
- Update Date:
- Nov 14 2011
- Associated Gene(s):
- EMILIN2
- Related URLs:
- NCBI dbSNP
EMILIN2 (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_032048
|
C1175G | NP_114437 | Missense | A392G |
