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CTSB (exon)
QuickView for rs149786664;jsessionid=008CF232260500845C3C0BA8BB602429 (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 8 : 11740066 (build 36.3)
- Strand:
- +
- Update Date:
- Nov 14 2011
- Associated Gene(s):
- CTSB
- Related URLs:
- NCBI dbSNP
CTSB (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_001908
|
G997C | NP_001899 | Missense | D333H |
|
NM_147780
|
G997C | NP_680090 | Missense | D333H |
|
NM_147781
|
G997C | NP_680091 | Missense | D333H |
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NM_147782
|
G997C | NP_680092 | Missense | D333H |
|
NM_147783
|
G997C | NP_680093 | Missense | D333H |
