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FGA (exon)
LOC100129857 (exon)
QuickView for rs138496061;jsessionid=78E4DF812D78C3439E47240052DB1359 (snp)
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Macaque
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Human
G|C
- Chimp
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Mouse
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Rat
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- Type:
- SNP
- Organism:
- Homo sapiens
- Alleles:
- G|C
- Chromosomal Location:
- chr 4 : 155726692 (build 36.3)
- Strand:
- +
- Update Date:
- Nov 14 2011
- Associated Gene(s):
- FGA, LOC100129857
- Related URLs:
- NCBI dbSNP
FGA (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000508
|
G1339C | NP_000499 | Missense | E447Q |
|
NM_021871
|
G1339C | NP_068657 | Missense | E447Q |
LOC100129857 (exon)
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
XM_001725995
|
C266G | XP_001726047 | Missense | S89C |
