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FYN (exon)
QuickView for rs138034632;jsessionid=48DB068966540EAD47BA9C93CD384FF2 (snp)
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Macaque
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Human
T|C
- Chimp
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Mouse
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Rat
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- Type:
- SNP
- Organism:
- Homo sapiens
- Alleles:
- T|C
- Chromosomal Location:
- chr 6 : 112122396 (build 36.3)
- Strand:
- +
- Update Date:
- Nov 14 2011
- Associated Gene(s):
- FYN
- Related URLs:
- NCBI dbSNP
FYN (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_002037
|
G1148A | NP_002028 | Missense | R383H |
|
NM_153047
|
G1139A | NP_694592 | Missense | R380H |
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NM_153048
|
G983A | NP_694593 | Missense | R328H |
